Not Logged In Log In   Sign Up   Points Leaders
Follow Us    9:02 PM

Message Forum - Read Message

Category: Off Topic > Topics Add to favorite topics   Post new topicPost New Topic
Author Topic: Food Recall Back to Topics
hawaii5oh

Champion Author
Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Mar 13, 2010 5:17:27 AM

Hydrolyzed Vegetable Protein (HVP), a flavor enhancer, made by one particular company is currently and albeit silently being recalled. The FDA has a pdf file indicated the products that uses HVP from this one company.

There is a potential, and I stress POTENTIAL, recall of more food items. Here in Hawaii a particular Red Potato Salad sold at Safeway's and Tim's Cascade Maui Onion Potato Chips were recalled.

FDA Link of recalled items Click on "View entire list..." to see the pdf table of possible recalled food items.
REPLIES (newest first) Post a Reply
Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 26, 2014 6:57:47 AM


Class I Recall 054-2014
Health Risk: High

California Firm Recalls Chicken Caesar Salad Kits For Possible Listeria Contamination

WASHINGTON, AUG. 21, 2014 – APPA Fine Foods, a Corona, Calif. establishment, is recalling approximately 92,657 pounds of fully cooked chicken Caesar salad kit products due to concerns about possible Listeria monocytogenes (Lm) contamination, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The salad kits were shipped nationwide to one bulk warehouse chain for retail sale in its in-store cafés. [APPA Fine Foods produced the kits used by the bulk warehouse chain.] The following products are subject to recall:

11oz. clear plastic containers and 6.5-lb. boxes labeled, “APPA Fine Foods/Sam’s Club Daily Chef CHICKEN CAESAR SALAD KIT” with case codes 141851, 141922, 141951, 141991, 142021, 142201 or 142131 with use by dates of 8/14/14, 8/21/14, 8/27/14, 9/1/14, 9/3/14 or 9/17/14. The kits were produced on July 4, July 11, July 14, July 18, July 21, July 25, Aug. 1 and Aug. 8, 2014.

Box labels bear the establishment number “P-21030” inside the USDA mark of inspection.

Michigan Department of Agriculture and Rural Development personnel informed FSIS they received two confirmed positive Lm results from retail product purchased at one of the bulk warehouse chain locations. The bulk warehouse chain then sampled intact components of the salad kits. Only the chicken came up positive with Lm.

FSIS and the company have received no reports of illnesses associated with consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-054-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 24, 2014 5:51:48 AM


Nestlé Prepared Foods Company Announces Allergy Alert and Voluntary Recall
Of LEAN CUISINE® Culinary Collection Chicken with Peanut Sauce Recall Due to Package Mislabeling

FOR IMMEDIATE RELEASE - August 22, 2014 - Nestlé Prepared Foods Company, a business unit of Nestlé USA, is initiating the voluntary recall of a limited quantity of LEAN CUISINE® Culinary Collection Chicken with Peanut Sauce/UPC code 13800 10154 because it may contain undeclared shrimp. People who have an allergy or severe sensitivity to shrimp run the risk of serious or life-threatening allergic reaction if they consume these products.

The affected product is marked with a production code of 4165595911U and has a “best before” date of JULY 2015. A small quantity of LEAN CUISINE Culinary Collection Shrimp Alfredo was inadvertently placed into packaging for LEAN CUISINE Culinary Collection Chicken with Peanut Sauce.

Three consumers who purchased the mislabeled product alerted Nestlé to this issue. To date, no illnesses or allergic reactions have been reported. Nestlé issued this voluntary recall of one hour code of production to ensure the safety of consumers with shellfish allergies.

http://www.fda.gov/Safety/Recalls/ucm411170.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 20, 2014 7:45:19 AM


nSPIRED Natural Foods, Inc. Voluntarily Recalls Certain Retail Lots Of Arrowhead Mills® Peanut Butters, Maranatha® Almond Butters And Peanut Butters And Specific Private Label Nut Butters Because Of Possible Health Risk

FOR IMMEDIATE RELEASE - August 19, 2014 - nSpired Natural Foods, Inc. is voluntarily recalling certain retail lots of Arrowhead Mills® Peanut Butters, MaraNatha® Almond Butters and Peanut Butters and specific private label nut butters (click on link below) packaged in glass and plastic jars because they have the potential to be contaminated with Salmonella.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and those with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

The potential risk was brought to the Company’s attention by the U.S. Food and Drug Administration following routine testing. The Company has received reports of four illnesses that may be associated with these specific products.

http://www.fda.gov/Safety/Recalls/ucm410533.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 17, 2014 6:46:33 AM


Voluntary Recall Notice of McCormick Ground Oregano Due to Possible Salmonella Risk

FOR IMMEDIATE RELEASE - August 13, 2014 - SPARKS, Md., August 13, 2014- McCormick & Company, Incorporated is initiating a voluntary recall of McCormick® Ground Oregano, 0.75 oz bottle, UPC 0-523561-6 with code dates BEST BY AUG 21 16 H and AUG 22 16 H due to possible contamination with Salmonella. This recall does not impact any other McCormick Ground, Whole or Oregano Leaves products.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses.

No illnesses have been reported to date in connection with this problem.

The product subject to this recall is:

McCormick® Ground Oregano 0.75 oz bottle
UPC NUMBER: 52100003566 (as seen on label: 0-523561-6)
MCCORMICK ITEM NUMBER: 900356
AFFECTED DATE CODES: BEST BY AUG 21 16 H, BEST BY AUG 22 16 H
SHIPPING DATES: April 4, 2014 to August 5, 2014
STATES SHIPPED TO: AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV

INTERNATIONALLY SHIPPED TO: Aruba, Bahamas, Bermuda, Indonesia, Jamaica, Netherlands, Puerto Rico, Singapore, Thailand, and Virgin Islands

The potential risk was brought to McCormick’s attention by FDA during routine testing. This recall affects 1,032 cases that were shipped of the affected date codes.

McCormick has alerted customers and grocery outlets to remove the product with the affected date codes from store shelves and distribution centers immediately, and to destroy this product in a manner that would prevent any further consumption.

http://www.fda.gov/Safety/Recalls/ucm410107.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 17, 2014 6:43:24 AM


Massachusetts Firm Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination

WASHINGTON, Aug. 15, 2014 – Whole Foods Market locations, South Weymouth, Mass. and Newton, Mass., are recalling 368 pounds of ground beef products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

125 lbs. of the following ground beef products produced on June 8, 2014 at the Newton, Mass. location are subject to recall (click on link below).

170 lbs. of the following ground beef products produced on June 10, 2014 at the Newton, Mass. location are subject to recall (click on link below).

73 lbs. of the following ground beef products produced on June 21, 2014 at the South Weymouth, Mass. location are subject to recall (click on link below).

FSIS was notified of an investigation of E. coli O157:H7 illnesses on June 25, 2014. Working in conjunction with the Massachusetts Department of Public Health and the Centers for Disease Control and Prevention (CDC), FSIS determined that there is a link between ground beef purchased at Whole Foods Market and this illness cluster. Based on epidemiologic investigation, 3 case-patients have been identified in Massachusetts with illness onset dates ranging from June 13, 2014 to June 25, 2014. While the onset of illnesses was in June, on August 13, 2014, additional laboratory results provided linkages between the 3 MA case-patients and ground beef purchased from Whole Foods. Traceback investigation indicated that all 3 case-patients consumed ground beef purchased from 2 Whole Foods Market prior to illness onset. FSIS is continuing to work with state and federal public health partners on this investigation to determine a common source and will provide updated information as it becomes available.

E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately.

FSIS and the company are concerned that some product may be frozen and in consumers' freezers.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-053-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 14, 2014 8:13:57 AM


Sunfood Recalls Organic Carob Powder Because Of Possible Health Risk

FOR IMMEDIATE RELEASE – August 11, 2014 – Sunfood of El Cajon, CA is recalling Organic Carob Powder, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

Organic Carob Powder was distributed nationwide in retail stores and through mail orders.

The product comes in 1lb, 20lb & 55lb white poly bags. The following lot numbers were affected: 140321,140416,140509,140516,140609,140616 & 140623. Expiration date is 6/5/2015 and UPC Code 803813-04429 8.

No illnesses have been reported to date in connection with this problem.

The potential for contamination was noted after routine testing by our supplier revealed the possibility of Salmonella in the above noted lot numbers.

http://www.fda.gov/Safety/Recalls/ucm409694.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 14, 2014 8:05:43 AM


Georgia Firm Recalls Chicken Nugget Product Due To Possible Foreign Matter Contamination

Class II Recall 052-2014
Health Risk: Low

WASHINGTON, Aug. 12, 2014 – Perdue, a Gainesville, Ga. establishment, is recalling approximately 15,306 pounds of frozen, fully cooked chicken nugget product that may be contaminated with extraneous materials, the U.S. Department of Agriculture’s FSIS announced today.

8-oz. box of “APPLEGATE naturals CHICKEN NUGGETS” bearing the establishment number “P2617” and the “BEST BEFORE” date of “02/05/15”.

The product was produced on Feb. 5, 2014, with a sell by date of Feb. 5, 2015 and bear the establishment number “P2617” inside the USDA Mark of Inspection. The products were shipped to retail outlets nationwide.

The problem was discovered after the firm received consumer complaints that small pieces of plastic were found in the products. FSIS and the company have received no reports of injury or illness from consumption of the product. Anyone concerned about an injury or illness from consumption of these products should contact a healthcare provider.

Applegate conducted a market withdrawal of this product on Aug. 8, 2014. However, as this is a frozen product, consumers may still have this product in their possession.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-052-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 14, 2014 8:00:06 AM


Recall Notification Report 051-2014
Class III Recall 051-2014

WASHINGTON, August 9, 2014 – Oberto’s Brands, a Kent, Wa. establishment, is recalling approximately 57,578 pounds of chicken strip products due to company quality issues, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The products subject to recall includes:

3, 5.75 and 16 oz. film bags of “Smokey Sweet BBQ Style Chicken Strips”

2.75, 3, 5.75, 9 and 16 oz. film bags of “Spicy Buffalo Style Chicken Strips”

The Smokey Sweet BBQ Style Chicken Strips were first produced on May 14, 2014 and last packaged on July 28, 2014. The Spicy Buffalo Style Chicken Strips were first produced on May 16, 2014 and last packaged on August 6, 2014. The product bears the establishment number “P4837” on the package. The product was sent to retail establishments nationwide as well as internet sales.

The problem was discovered by the company. A sister establishment noticed bloated packages and alerted the company to the problem. The plant determined that the increased water activity is due to “an undetected process deviation.” The establishment further stated the product met all critical limits during production. The company has determined that this a quality control issue and that there are no food safety hazards.

FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/rnr-051-2014

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 7:13:35 AM


The next three posts appeared in the FDA Recall list so I have included it in this forum.

Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Nine Lots of CUBICIN (daptomycin for injection) 500 mg in 10 mL single use vials Following Complaints of Foreign Particulate Matter in Reconstituted Vials

FOR IMMEDIATE RELEASE – August 8, 2014 – Cubist Pharmaceuticals, Inc.disclaimer icon (NASDAQ: CBST) today announced it is voluntarily recalling nine lots of CUBICIN® (daptomycin for injection) to the user level following complaints of foreign particulate matter in reconstituted vials.

The administration of particulate matter, if present in an intravenous drug, poses a potential safety risk to patients such as a thromboembolism or a life-threatening pulmonary embolism. Other events such as phlebitis, mechanical block of the capillaries or arterioles, activation of platelets or subsequent generation of microthrombi are also possible. Patients with a preexisting condition of trauma or other medical condition that adversely affects the microvascular blood supply are at an increased risk. Administration of a particulate can also lead to formation of granulomas, which represent a protective local inflammatory response to the foreign material. To date, no reports of adverse events have been associated with product complaints of particulate matter from these lots.

Cubist is notifying customers by letter and phone. Anyone with an existing inventory of the product lots listed should determine whether they have product from the recalled lots, quarantine, and discontinue distribution of these recalled lots of the product and call Cubist at (855) 534-8309 between the hours of 9 a.m. to 7 p.m. EDT, Monday through Friday, to arrange for return and replacement of the affected lots.

http://www.fda.gov/Safety/Recalls/ucm408928.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 7:11:48 AM


Cubist Pharmaceuticals Issues Voluntary U.S. Recall Of Certain Lots Of CUBICIN (Daptomycin For Injection) 500 mg In 10 mL Single Use Vials Due To Presence Of Particulate Matter

FOR IMMEDIATE RELEASE - August 6, 2014 - Cubist Pharmaceuticals, Inc. (NASDAQ: CBST) today announced it is voluntarily recalling certain lots of CUBICIN® (daptomycin for injection) to the user level due to the potential presence of glass particulate matter in vials produced by a contract manufacturer. Please click heredisclaimer icon for the list of affected CUBICIN lot information.

The administration of a glass particulate, if present in an intravenous drug, poses a potential safety risk to patients such as a thromboembolism or a life-threatening pulmonary emboli. Other events such as phlebitis, mechanical block of the capillaries or arterioles, activation of platelets, or subsequent generation of microthrombi are also possible. Patients with a preexisting condition of trauma or other medical condition that adversely affects the microvascular blood supply are at an increased risk. Administration of a glass particulate can also lead to formation of granulomas, which represent a protective local inflammatory response to the foreign material.

Cubist has decided to issue a voluntary recall of these lots as a result of an issue with a manufacturing line of one of our suppliers that could result in glass particulate matter in vials. No complaints of glass in vial or adverse events in association with a product complaint of glass in vial have been reported to date for these recalled lots.

CUBICIN is an intravenously administered prescription product indicated for the treatment of skin infections and certain blood stream infections. CUBICIN is supplied in a single-use vial packaged in a carton. CUBICIN was distributed nationwide to multiple consignees.

Cubist is notifying customers by letter and phone. Anyone with an existing inventory of the product lots listed should determine whether they have product from the recalled lots, quarantine, and discontinue distribution of this recalled lots of the product and call Cubist at (855) 534-8309 between the hours of 9 a.m. to 7 p.m. EDT, Monday through Friday, to arrange for return and replacement of the affected lots.

http://www.fda.gov/Safety/Recalls/ucm408576.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 7:07:23 AM


Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegeneSlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk

FOR IMMEDIATE RELEASE – August 6, 2014 – Regeneca Worldwide a division of VivaCeuticals, Inc. Las Vegas, NV is conducting a voluntary nationwide recall of its RegeneSlim appetite control dietary supplement from lot # EX0616R15814 and lot #11414RE5516 because FDA analysis confirmed the presence of DMAA. DMAA is also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract. DMAA is commonly used as a stimulant, pre-workout, and weight loss ingredient in dietary supplement products. The Food and Drug Administration (FDA) has warned that DMAA is potentially dangerous to health as it can narrow blood vessels and arteries, which can cause a rise in blood pressure or other cardiovascular problems such as shortness of breath, arrhythmias, tightening in the chest, and heart attack.

RegeneSlim is purchased by and distributed through a direct sales force within the United States and Puerto Rico, and through online sales, for both personal consumption and retail sales.

RegeneSlim is packaged in approximately 3 ½” by 3” green and white sachets that contain 2 capsules, with the name RegeneSlim displayed prominently on the front of the sachet.

There have been no illnesses reported to date.

This voluntary recall was the result of FDA analysis confirming the presence of DMAA in RegeneSlim and our company’s sampling. The company continues their investigation as to what caused the problem.

http://www.fda.gov/Safety/Recalls/ucm408674.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 6:54:04 AM


Seoul Shik Poom Inc. Issues Allergy Alert on Undeclared Eggs in Choripdong Chocolate Almond Richmond Ice Bar

FOR IMMEDIATE RELEASE - August 5, 2014 - Seoul Shik Poom Inc. of Englewood, NJ is recalling Choripdong Chocolate Almond Richmond Ice Bar (4bags/432ml) because they may contain undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.

The recalled Choripdong Chocolate Almond Richmond Ice Bar(4bars/432 ml) was distributed nationwide through retail stores.

Choripdong Chocolate Almond Richmond Ice Bar (4bars/432 ml) was sold in a silver plastic cooling bag marked with code # IC1006 and UPC CODE: 761898632925. The product has an expiration date of 03/20/2015 which is stamped on the package.

No illnesses have been reported to date in connection with this problem.

http://www.fda.gov/Safety/Recalls/ucm408027.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 6:47:30 AM


Recall Notification Report 051-2014

Class III Recall 051-2014

WASHINGTON, August 9, 2014 – Oberto’s Brands, a Kent, Wa. establishment, is recalling approximately 57,578 pounds of chicken strip products due to company quality issues, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The products subject to recall includes:

3, 5.75 and 16 oz. film bags of “Smokey Sweet BBQ Style Chicken Strips”

2.75, 3, 5.75, 9 and 16 oz. film bags of “Spicy Buffalo Style Chicken Strips”

The Smokey Sweet BBQ Style Chicken Strips were first produced on May 14, 2014 and last packaged on July 28, 2014. The Spicy Buffalo Style Chicken Strips were first produced on May 16, 2014 and last packaged on August 6, 2014. The product bears the establishment number “P4837” on the package. The product was sent to retail establishments nationwide as well as internet sales.

The problem was discovered by the company. A sister establishment noticed bloated packages and alerted the company to the problem. The plant determined that the increased water activity is due to “an undetected process deviation.” The establishment further stated the product met all critical limits during production. The company has determined that this a quality control issue and that there are no food safety hazards.

FSIS and the company have received no reports of adverse reactions due to consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/rnr-051-2014

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 10, 2014 6:44:58 AM


New York Firm Recalls Sausage Product Due To Misbranding and Undeclared Allergen

Class I Recall 050-2014
Health Risk: High

WASHINGTON, August 6, 2014 – Zemco Industries Inc., a Buffalo, NY, establishment, is recalling approximately 106,800 pounds of smoked sausage due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains soy, a known allergen that is not declared on the label of the product.

The product subject to recall includes:

2.5 lb. packages of “CAVANAUGH SMOKED SAUSAGE”

The products were produced on June 11, 2014; June 13, 2014; June 19, 2014; July 10, 2014; July 19, 2014; and Aug. 1, 2014. The recalled product has Use By dates of Sept. 9, 2014; Sept. 11, 2014; Sept. 17, 2014; Oct. 8, 2014; Oct. 17, 2014; and Oct. 30, 2014. The product bears the establishment number “Est. 5222” on the package. The product was sent to distribution centers for resale as well as retail establishments nationwide.

The problem was discovered by the company. The problem occurred when the company reformulated the product and updated packaging and labeling but the employees utilized the old formulation containing soy that was not declared on the updated packaging and labels. FSIS and the company have received no reports of adverse reactions due to consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-050-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:35:49 AM


New England Greens, LLC dba Vibrant Health Recalls Green Vibrance and Rainbow Vibrance Because of Possible Health Risk

FOR IMMEDIATE RELEASE - August 1, 2014 - New England Greens of Canaan, Connecticut is recalling 10 lots of Green Vibrance and one lot of Rainbow Vibrance after a former raw material supplier, Raw Deal of Allamuchy, NJ, recalled the Organic Parsley Leaf Powder used to manufacture Green Vibrance and Rainbow Vibrance because of the potential for contamination with Salmonella. Although the possibility is slight that any amount of Salmonella is present in any of the recalled lots of the above-mentioned products, New England Greens is issuing the recall with an abundance of caution for the safety of its consumers. No illnesses have been reported to date in connection with this problem.

The implicated lots of Green Vibrance and Rainbow Vibrance were distributed nationwide through both brick and mortar and online health food and natural product retailers. The products are packaged in white, high density polyethylene (HDPE) canister jars ranging in size from 20 ounce to 51 ounce. One lot of Green Vibrance capsules, 240 per bottle, is also included in the recall as well as one lot of Green Vibrance single-serving packets, 15 packets per cardboard display box.

To date, Vibrant Health has received NO COMPLAINTS and there have been NO INCIDENTS of salmonellosis related to any lot number of Green Vibrance or Rainbow Vibrance.

http://www.fda.gov/Safety/Recalls/ucm407801.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:34:21 AM


Sunburst Superfoods Recalls Organic Raw Carob Powder Because of Possible Health Risk

FOR IMMEDIATE RELEASE - August 1, 2014 - Sunburst Superfoods of Tuckahoe, NY, is recalling Sunburst SUPERFOODS Organic Raw Carob Powder sold from March 12, 2014 through July 28th, 2014, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

Sunburst SUPERFOODS Organic Raw Carob Powder was distributed throughout the United States to consumers through online sales.

Sunburst SUPERFOODS Organic Raw Carob Powder was sold in One Pound and Five Pound bags with no coding. The product is packaged in re-sealable, all-natural brown paper bags with a thin metal and thin plastic lining on the interior of the bags.

No illnesses associated with this product have been reported to date.

http://www.fda.gov/Safety/Recalls/ucm407794.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:33:25 AM


Wawona Packing Co. Expands Its Voluntary Recall of Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk

FOR IMMEDIATE RELEASE - July 31, 2014 - Out of an abundance of caution, Wawona Packing Company of Cutler, California is expanding its voluntary recall from July 19, 2014, of whole white and yellow peaches, white and yellow nectarines, plums and pluots due to the potential of the products being contaminated with Listeria monocytogenes.

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The July 19 recall covered specific lots of products packed from June 1 through July 12, 2014. Wawona Packing Company is expanding the recall, as a precautionary step, to cover all products packed in the Wawona Packing Co. facility from June 1, 2014 through July 17, 2014 because the company’s experts have yet to identify with scientific certainty the source of Listeria monocytogenes in the facility.

Beginning on July 18, 2014, no products have been packed at the Wawona Packing facility in Cutler, CA. Products packed on or after July 18 outside of the Wawona Packing Co. facility are not affected by this recall.

http://www.fda.gov/Safety/Recalls/ucm407600.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:32:24 AM


CDPH Warns Consumers Not to Eat VR Green Farms Jarred Food Products Because of Botulism Risk

FOR IMMEDIATE RELEASE - July 30, 2014 - California Department of Public Health (CDPH) Director and State Health Officer Dr. Ron Chapman warned consumers today not to eat VR Green Farms jarred food products because they may have been improperly produced, making them susceptible to contamination with Clostridium botulinum.

Ingestion of botulism toxin from improperly processed jarred and canned foods may lead to serious illness and death. CDPH is coordinating with the US Food and Drug Administration and the Ohio Department of Health in the investigation of two cases of suspected food-borne botulism infections that may be associated with consumption of the firm’s Pine Nut Basil Pesto.

VR Green Farms of San Clemente, California, is voluntarily recalling the following varieties of jarred food products: Pine Nut Basil Pesto, Pickled Farm Mix, Old World Tomato Sauce, Sundried Tomatoes in Olive Oil, Tuscan Grilling Sauce, and Pasta Sauce. These food products were sold under the VR Farms label and packaged in Mason-style glass jars with screw-on metal lids. The product labels do not include any coding or “use by” dates. Photographs can be found on Recalled Product Photos Page. The products were sold at the VR Green Farms stand in San Clemente, California and via the Internet to consumers throughout the United States.

Botulism toxin is odorless and colorless. Consumers who have any of these products or any foods made with these products should discard them immediately. Double bag the cans in plastic bags and place in a trash receptacle for non-recyclable trash. Wear gloves when handling these products or wash your hands with soap and running water.

http://www.fda.gov/Safety/Recalls/ucm407542.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:31:18 AM


Natural Grocers by Vitamin Cottage Issues Voluntary Recall For Various Chunks of Energy Products Because They Contain Organic Carob Powder From Ciranda, Inc., Which May Be Contaminated With Salmonella

FOR IMMEDIATE RELEASE - July 29, 2014 - Lakewood, CO. Natural Grocers is issuing a voluntary recall of Chunks of Energy Carob Greens and Chunks of Energy Date / Flax/Tumeric because they contain organic carob powder from Ciranda, Inc., Hudson, WI 54016, which may be contaminated with Salmonella.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infection (i.e., infected aneurysms), endocarditis and arthritis.

Products impacted by the recall include Natural Grocers bulk food brand labeled as follows:

CHUNKS OF ENERGY CAROB GREENS
Packed On dates: 155-14, 167-14, 175-14

CHUNKS OF ENERGY DATE / FLAX /TUMERIC
Packed On dates: 125-14, 133-14, 147-14, 155-14, 170-14, 181-14

Packed On dates appear near the bottom of the label affixed to each bag.

These products were repackaged by Natural Grocers and sold in small bags in the refrigerated bulk foods section of the stores. A black and white printed label is affixed to each bag. The product was distributed only to Natural Grocers’s 84 stores located in Arizona, Colorado, Idaho, Kansas, Missouri, Montana, Nebraska, New Mexico, Oklahoma, Oregon, Texas, Utah, Washington and Wyoming.

No illnesses have been reported to date in connection with this problem.

http://www.fda.gov/Safety/Recalls/ucm407197.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Aug 3, 2014 5:30:13 AM


SW Wisc Dairy Goat Products Coop issues voluntary recall of Raw Goat Milk Mild Cheddar Cheese Lot Code 103-114 because of possible health risk

FOR IMMEDIATE RELEASE – July 28, 2014 – SW Wisc Dairy Goat Products Coop of Mt Sterling, Wisc is recalling Raw Milk Mild Cheddar Cheese Lot Code 103-114 because it may be contaminated with Shiga toxin producing Escherichia coli (STEC) O111:H8 bacteria. This is one of the 6 STEC strains that have been deemed to be of serious health concern as it can cause diarrheal illness, often with bloody stools, and may lead to more severe complications like Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children, the elderly and immunocompromised individuals and can lead to severe kidney damage and even death.

This product was distributed in the Midwest and Southwest regions of the US. This product was sent through distributorship in Wisconsin and Georgia. From these two states this product was then sent to retail stores in the Midwest and Southwest.

The recall was initiated after a case of two five pound loafs in the original packaging was collected on 7-8—14 from an offsite warehouse. The product sample tested positive for Shiga toxin 1and was contaminated with E. coli O111:H8.

http://www.fda.gov/Safety/Recalls/ucm407355.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 31, 2014 7:17:51 AM


Massachusetts Firm Recalls Raw Boneless Turkey Breasts Due To Misbranding and Undeclared Allergen

WASHINGTON, July 26, 2014 – Puritan Foods Co., Inc., a Boston, Mass., establishment, is recalling approximately 2,476 pounds of raw boneless turkey breasts due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk, a known allergen, which is not declared on the product label.

The following product is subject to recall:

Raw Boneless Turkey Breasts (various weights) with pack dates of June 11 and July 18, 2014

The product was produced on June 11, 2014, and July 18, 2014, and bears the establishment number “P-5933” inside the USDA mark of inspection. The product was distributed to a local distributor, which sold the product to hotels, restaurants and institutions in the New England area.

FSIS personnel discovered the problem while checking product labels. The source materials typically used by the firm do not contain milk. On the two dates in question, the source materials used declared they were “butter basted,” which was not carried over to the finished product label. Milk is a sub-ingredient in butter and must be noted on the label.

FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-049-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 31, 2014 7:15:22 AM


Hummingbird Wholesale Recalls Organic Raw Carob Powder for Possible Salmonella Contamination

FOR IMMEDIATE RELEASE -July 29, 2014 – Hummingbird Wholesale in Eugene Oregon has been notified by its supplier of a recall of Organic Raw Carob Powder due to possible health risks related to potential Salmonella contamination. Salmonella is an organism which can cause serious and sometime fatal infections in young children, frail, or elderly people and others with weakened immune systems.

Hummingbird Wholesale has taken immediate action to recall the Organic Raw Carob Powder in order to ensure the safety of its consumers. Hummingbird Wholesale is working closely with the FDA on this matter. Hummingbird Wholesale is dedicated to providing the highest quality organic and raw products, and the safety of our customers is our number one priority.

Products in question were sold to processors and retail outlets in Oregon, Washington, and California and to the end consumer in Oregon in 20 lb boxes and 5 lb bags between the dates of 5/22/14 through 7/24/14.

No other Hummingbird Wholesale products are affected by this recall and no illnesses have been reported to date. This recall is initiated as a precautionary measure due to a possibility of contamination as notified by our suppliers.

http://www.fda.gov/Safety/Recalls/ucm407221.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 31, 2014 7:13:13 AM


SW Wisc Dairy Goat Products Coop issues voluntary recall of Raw Goat Milk Mild Cheddar Cheese Lot Code 103-114 because of possible health risk

FOR IMMEDIATE RELEASE – July 28, 2014 – SW Wisc Dairy Goat Products Coop of Mt Sterling, Wisc is recalling Raw Milk Mild Cheddar Cheese Lot Code 103-114 because it may be contaminated with Shiga toxin producing Escherichia coli (STEC) O111:H8 bacteria. This is one of the 6 STEC strains that have been deemed to be of serious health concern as it can cause diarrheal illness, often with bloody stools, and may lead to more severe complications like Hemolytic Uremic Syndrome (HUS). HUS is most likely to occur in young children, the elderly and immunocompromised individuals and can lead to severe kidney damage and even death.

This product was distributed in the Midwest and Southwest regions of the US. This product was sent through distributorship in Wisconsin and Georgia. From these two states this product was then sent to retail stores in the Midwest and Southwest.

This product was packed as an 8oz cryovac retail size piece with the code 103-114 on a sticker attached to the side of the cheese. This product is all white in appearance and has a front and back separate label. The back label is a black and white nutrition and ingredient label and the front label is a yellow and blue colored label with the Mt Sterling Coop Creamery brand name. "No illnesses have been reported to date."

The recall was initiated after a case of two five pound loafs in the original packaging was collected on 7-8—14 from an offsite warehouse. The product sample tested positive for Shiga toxin 1and was contaminated with E. coli O111:H8.

http://www.fda.gov/Safety/Recalls/ucm407355.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 29, 2014 8:23:47 AM


Something wrong with my links magpie2013? I just reviewed all of the links with the July 28th time stamp and they all came up with no problem.
Profile Pic
magpie2013
Champion Author Milwaukee

Posts:3,242
Points:133,755
Joined:Apr 2013
Message Posted: Jul 28, 2014 7:51:47 PM

Well that was odd the page said that they were no longer available about product recall! Makes you wonder how much else is being swept under the carpet!
Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:55:37 AM


The TJX Companies, Inc. Recalls "Ecoato" Sweet Paprika Powder Due to Possible Health Risk

FOR IMMEDIATE RELEASE - July 26, 2014 - Framingham, MA - The TJX Companies, Inc. today announced it is recalling “ecoato” Sweet Paprika Powder products as they have the potential to be contaminated with Salmonella. Upon learning of the potential risk from the Food and Drug Administration, the Company took rapid action to alert its stores to remove the product from store shelves immediately and has put in place additional measures to prevent sales of the product.

The specific product being recalled comes in a 160 gram, light green tin package and is marked as lot #8147, with an expiration date of October 2015.

The Company estimates that approximately 150 units were sold between June 2014 and July 2014 at its T.J. Maxx, Marshalls and HomeGoods stores in the followi ng 19 states/regions:

Alabama Connecticut District of Columbia Florida
Georgia Illinois Louisiana Maryland Massachusetts
Mississippi New Hampshire New York North Carolina Rhode Island
South Carolina Tennessee Texas Virginia Puerto Rico


While no illnesses have been reported to date in connection with this issue, consumers who have purchased a product under this lot of “ecoato” Sweet Paprika Powder are urged to return it to any T.J. Maxx, Marshalls or HomeGoods store for a full refund. Consumers with questions should contact the Company at 1-800-926-6299.

In addition to actions taken to remove the product from store shelves, further sale of the product has been suspended while the Food and Drug Administration and the Company continue their investigation as to the source of the problem.

http://www.fda.gov/Safety/Recalls/ucm406812.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:49:30 AM


Carmel Food Group Announces a Voluntary Recall of One Code Date of Mislabeled Butternut Squash Ravioli Due to Undeclared Allergens

FOR IMMEDIATE RELEASE - July 25, 2014 – Hayward, CA. Carmel Food Group today issued a voluntary recall of Rising Moon Organics Butternut Squash Ravioli, a frozen product, because of mixed product in the packages with SELL BY APR 09 2015 (ONLY). This mislabeling incident has resulted in product which may contain undeclared allergens, milk, egg, and soy. People who have an allergy or severe sensitivity to milk, egg, and soy run the risk of serious or life-threatening allergic reaction if they consume this product.

Product: Rising Moon Organics Butternut Squash Ravioli, 8 oz, UPC# 7-85030-55557-6. One Code Date is affected: Pkg. SELL BY APR 09 2015, Case SELL BY 040915 (ONLY this Sell By date is being recalled).

The product involved was distributed through retail stores nationwide.

The recall was initiated when it was discovered that some packages labeled Butternut Squash that contain ravioli pieces with a different filling that may include milk, egg, and soy ingredients.

No illnesses have been reported to date in association with this product.

http://www.fda.gov/Safety/Recalls/ucm406808.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:48:28 AM


CaCoCo, Inc. Recalls Raw Drinking Chocolate Containing Voluntarily Recalled Organic Carob Powder From Their Supplier for Possible Salmonella Contamination

FOR IMMEDIATE RELEASE - July 25, 2014 - CaCoCo, Inc. has been notified by its supplier of a recall of Organic Carob Powder due to possible health risks related to Salmonella contamination. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail, or elderly people and others with weakened immune systems.

CaCoCo, Inc. has taken immediate action to recall its products, CaCoCo “Original” and “Global Warrior” containing said Organic Carob Powder in order to ensure the safety of its consumers. CaCoCo, Inc. is working closely with the FDA on this matter. CaCoCo, Inc. is dedicated to providing the highest quality organic and raw products and the safety of our customers is our number one priority.

Products were sold to California distributors, retail outlets, and farmers markets in 8.14 oz. and 2 lbs. bags. The products in this recall include: (click on the link to view the recalled products)

No other CaCoCo, Inc. products are affected by this recall and no illnesses have been reported to date. This recall is initiated as a precautionary measure due to a possibility of contamination as notified by our suppliers.

Consumers that have purchased these products with the above stated lot numbers or expiration dates are asked not to consume the product and discard it according to your state/local regulation guidelines or return the product to the original point of purchase for exchange.

http://www.fda.gov/Safety/Recalls/ucm406806.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:46:42 AM


GOMACRO RECALLS "Almond Butter + Carob" and “Sunflower Butter + Chocolate” MacroBars Because of Possible Health Risk Carob Powder Supplier May Have Exposed Ingredient to Salmonella

FOR IMMEDIATE RELEASE - July 25, 2014 - GoMacro, of Viola, Wis., is recalling MARCOBARS brand almond butter + carob lots 1634 and 1645 and sunflower butter + chocolate lot 1646, because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

GoMacro was notified on July 23 by its supplier of carob powder, an ingredient in the company’s almond butter + carob bars, that one of their customers received a positive test for Salmonella. In the interest of abundant caution, GoMacro is voluntarily recalling lot 1646 of sunflower butter + chocolate because it was produced on the same line after lots 1634 and 1645. These MacroBars were distributed across the country and internationally via retail stores, mail order and direct delivery.

Affected MacroBars will be clearly marked as either almond butter + carob with lot numbers 1634 (expiration 10 Mar 15) or 1645 (expiration 18 Mar 15) or sunflower butter + chocolate lot 1646 (expiration 18 Mar 15) and in a foil wrapper.

No illnesses have been reported to date.

http://www.fda.gov/Safety/Recalls/ucm406804.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:37:08 AM


Lion Pavilion Issues Alert on Undeclared Sulfites in Tasty Peach Slices

FOR IMMEDIATE RELEASE - July 24, 2014 - LION PAVILION LTD. of Maspeth, NY is recalling Tasty Peach Slices because it contains undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

Tasty Peach Slices is sold in 3.87 ounce (110g), clear plastic jar and was distributed nationwide. It is a product of China.

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 110g package of Tasty Peach Slices which were not declared on the label. The consumption of 10 milligrams of sulfites per serving has been reported to elicit severe reactions in some asthmatics. Anaphylactic shock could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites. Analysis of the Tasty Peach Slices revealed they contained 12.75 milligrams per serving.

No illnesses or allergic reactions involving this product have been reported to date.

http://www.fda.gov/Safety/Recalls/ucm406623.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:35:53 AM


Dancing Star LLC, Buckland, MA 01338 Issues Voluntary Recall For Various Snacks Because They Contain Organic Carob Powder From Ciranda, Inc., Hudson, WI 54016, Which May Be Contaminated With Salmonella.

FOR IMMEDIATE RELEASE - July 24, 2014 - Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infection (i.e., infected aneurysms), endocarditis and arthritis.

Products impacted by the recall include:

Dancing Star LLC brand: (click on the link to view the recalled products)

There are no other flavors of Dancing Star Chunks of Energy or Rave Bites being recalled

The recalled items are distributed nationwide and sold to retail stores, some of them in bulk for the sales of smaller quantities to their customers.

No illnesses have been reported to date in connection with this problem.

Consumers who have purchased this item are urged to not eat the product, and to dispose of it or return it to the store where it was originally purchased for credit.

http://www.fda.gov/Safety/Recalls/ucm406771.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:33:48 AM


Texas Firm Recalls Ready-to-eat Products For Possible Listeria Contamination

FOR IMMEDIATE RELEASE - July 24, 2014 - Great American Marketing, a Houston, Texas establishment, is recalling approximately 475 pounds of FSIS and FDA-regulated, ready-to-eat products due to possible contamination with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The sandwich and wrap products were produced on July 15, 2014, and then shipped to retail locations in Texas. Case labels or packaging bear the sell by date of 07/26/14.

Products regulated by FSIS bear the establishment number “EST 31680” or “P-31680” inside the USDA mark of inspection. The following FSIS-regulated products are subject to recall:

7.4 ounce plastic-covered tray packages containing Chicken Caesar Wraps.
8.1 ounce plastic-covered tray packages containing Club Wraps.

FDA-regulated products being recalled (are listed at http://www.fda.gov/safety/recalls/) and include:

10.5 ounce plastic-covered tray packages containing Ham and Cheddar Premium sandwiches.
10.5 ounce plastic-covered tray packages containing Turkey & Swiss Premium sandwiches.

The problem was discovered when FSIS collected a sample of a separate product on July 15, 2014, that was confirmed positive for L. monocytogenes on July 23. The sampled product was held. However, the plant produced the additional FSIS and FDA regulated products listed in this recall without conducting a complete clean-up of the production equipment. Those products have entered commerce and are subject to recall. FSIS and the company have received no reports of illnesses associated with consumption of these products.

http://www.fda.gov/Safety/Recalls/ucm406736.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:30:23 AM


Whole Foods Market Recalls Made-In-Store Items Prepared With Stone Fruit Voluntarily Recalled by Wawona Packing Co. Due to Possible Health Risk

FOR IMMEDIATE RELEASE - AUSTIN, Texas - July 23, 2014 – Whole Foods Market has recalled made-in-store items prepared with organic and conventional stone fruit, including peaches, nectarines, and plums from Wawona Packing Co. because of possible contamination with Listeria monocytogenes.

While no illnesses have been reported to-date, Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Made-in-store items that contained one or more fruits subject to the Wawona Packing Co. recall were sold between June 1st and July 21st. Not all items or all products were sold in all store locations. Affected made-in-store items such as cakes, tarts, salsas, and prepared salads were sold in Whole Foods Market stores using Whole Foods Market scale labels in all states where Whole Foods Market stores are located except Florida, Washington and Oregon. Additionally, Whole Foods Market pulled and destroyed the recalled stone fruit sold in all regions where it was available, which may have been labeled with a “Sweet 2 Eat” sticker. For a list of made-in-store items that have been affected by state, please check this web page.

Whole Foods Market was notified by Wawona Packing Co. that the various stone fruits were recalled due to a positive test result for Listeria monocytogenes.

http://www.fda.gov/Safety/Recalls/ucm406461.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 28, 2014 8:28:52 AM


Earth Circle Organics Recalls Organic Carob Powder for Possible Salmonella Contamination

FOR IMMEDIATE RELEASE - July 22, 2014 - Earth Circle Organics, (River Canyon Retreat, Inc., dba) has been notified by its supplier of a recall of Organic Carob Powder due to possible health risks related to Salmonella contamination. Salmonella is an organism which can cause serious and sometime fatal infections in young children, frail, or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.

Earth Circle Organics has taken immediate action to recall Organic Carob Powder in order to ensure the safety of its consumers.

No other Earth Circle Organics products are affected by this recall and no illnesses have been reported to date. This recall is initiated as a precautionary measure due to a possibility of contamination as notified by our suppliers.

http://www.fda.gov/Safety/Recalls/ucm406458.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 15, 2014 8:00:33 AM


Not related to food or produce but this recall did appear in the FDA site.Voluntary Nationwide Recall of Tattoo Ink, Tattoo Needles, Tattoo kits Due to Microbial Contamination

FOR IMMEDIATE RELEASE - July 11, 2014 - July 11, 2014- White & Blue Lion, Inc. in the City of Industry, CA is recalling all lots of tattoo Inks and tattoo needles due to pathogenic bacterial contamination. Use of these products may cause bacterial infection and can lead to sepsis, a potentially life-threatening complication of an infection. The recall includes all tattoo inks, tattoo needles, and tattoo kits distributed by White & Blue Lion including the ones specifically listed below (click on the link below).

The inks and needles are sold in tattoo kits and the inks are also sold separately by 8Decades and White & Blue Lion, Inc. through www.amazon.com.

There was a report of one illness as of today’s date.

FDA Laboratory testing has found microbial bacterial contamination in both the inks and needles.

This recall is being made with the knowledge of the US Food and Drug Administration.

http://www.fda.gov/Safety/Recalls/ucm404787.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 15, 2014 7:57:54 AM

Charles Products Recalls Decorative Pint And Shot Glasses Due To Possible Health Risk

FOR IMMEDIATE RELEASE - May 22, 2014 - Charles Products, Inc. (CPI) announced today that it is voluntarily recalling shot and pint glasses identified below sold exclusively through M&M’S World retail stores in New York, Las Vegas, Orlando and London.

CPI is recalling the following shot and pint glasses:

Glasses with an image of the Red M&M’S character and the words “Hard on the outside, soft on the inside;”

Glasses with an image of the Blue M&M’S character and the words “Who’s your candy?;” and

Glasses with an image of the Green M&M’S character and the words “Eye candy.

Through its internal compliance and independent laboratory product testing program, the company became aware that the glassware may exceed the Food and Drug Administration’s (“FDA”) guidance levels for leachable lead and cadmium. Both lead and cadmium are heavy metals found in the environment that accumulate in human bodies. Both can cause serious health complications at high levels. These glasses should therefore be returned and should not be used for the consumption of beverages, alcoholic or otherwise.

1,202 pint glasses and 6,335 shot glasses have been sold between the dates of January 8, 2014 and April 16, 2014. No illness related to this product has been reported to date. The recall only applies to the SKU #s below and no other products are affected.

Picture of the recalled shot glasses: http://www.fda.gov/Safety/Recalls/ucm404577.htm

http://www.fda.gov/Safety/Recalls/ucm404573.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 15, 2014 7:55:41 AM


Whole Foods Market Recalls Pre-packaged Mini Caesar And Mini Mesclun Goat Cheese Salad In Three States, Due To Undeclared Allergen

FOR IMMEDIATE RELEASE - July 8, 2014 - Whole Foods Market is recalling mini 4oz. containers of pre-packaged Caesar salad and Mesclun Goat Cheese salad sold in stores on July 8,, 2014 throughout New York, New Jersey (Excluding Princeton, Cherry Hill and Marlton) and Connecticut (Excluding Glastonbury, West Hartford and Bishop’s Corner) due to mislabeling and a resulting undeclared allergen of fish and egg (Caesar) and tree nuts (Mesclun Goat Cheese). The product has a Sell by date of: 7/11/14.

The salad labels were erroneously swapped and therefore the Caesar Salad packages contain tree nuts and the Mesclun Goat Cheese packages contain a Caesar dressing containing fish and egg as an ingredient. People who have an allergy or severe sensitivity to any of these ingredients run the risk of serious or life-threatening allergic reaction if they consume these products.

Signage is posted in affected Whole Foods Market stores to notify customers of this recall, and all affected product has been removed from shelves.

http://www.fda.gov/Safety/Recalls/ucm404286.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 1, 2014 3:39:58 AM


Class II Recall 042-2014
Health Risk: Low

Pennsylvania Firm Recalls Deli Ham Product Due To Possible Foreign Matter Contamination

WASHINGTON, June 27, 2014 – E. G. Emils & Sons, Inc., a Philadelphia, Pa. establishment, is recalling approximately 5,896 pounds of deli ham product that may be contaminated with extraneous materials, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The following product is subject to USDA recall:

"Wegman’s Food You Feel Good About Organic Ham,” Wegman’s Private Label with pack lot numbers 14941309, 14941310 and 14941311.

This product bears “EST 9935” inside the USDA mark of inspection on the labels and was produced May 29, 2014. The product was shipped to Wegman’s locations in Maryland, Massachusetts, New Jersey, New York, Pennsylvania and Virginia to be sliced at deli counters. The organic ham was sold between June 12 and June 25.

The problem was discovered by a Wegman’s employee upon slicing the ham at the deli counter. The problem was traced to a piece of plastic that broke off from an interlocker belt.

Neither the company nor FSIS has received any reports of injury associated with consumption of this product.

http://www.fsis.usda.gov/wps/wcm/connect/FSIS-Content/internet/main/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-042-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 1, 2014 3:35:47 AM


Richard’s Rubs & Seasonings Recalls Sauces Because of Possible Health Risk

FOR IMMEDIATE RELEASE - June 27, 2014 - Richard’s Rubs & Seasonings LLC is recalling Richard’s Too Good BBQ Sauce, Richard’s Too Good Hot Sauce and Richard’s Too Good Teriyaki Sauce because they may have been improperly processed and because they may have the potential to be contaminated with Clostridium botulinum, which can cause botulism, a serious and potentially fatal foodborne illness.

Foodborne botulism is a severe type of food poisoning caused by the ingestion of foods containing the potent neurotoxin formed during growth of the organism. Foodborne botulism can cause the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing. Difficulty in breathing, weakness of other muscles, abdominal distension and constipation may also be common symptoms. People experiencing these problems should seek immediate medical attention. Consumers are warned not to use the product even if it does not look or smell spoiled.

The recalled sauces were sold in western Washington grocery stores and butcher shops in Kitsap, Snohomish and King counties.

Sauces are packaged in 12 oz tall glass bottles with metal screw caps and black heat resistant tamper seals.

The products being recalled were distributed up to the date of June 17, 2014. This recall has been initiated because of a consumer complaint indicating that sauce may have been improperly processed. Richard’s Rubs & Seasonings LLC has not been notified of any illness associated with their products.

http://www.fda.gov/Safety/Recalls/ucm403200.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 1, 2014 3:34:28 AM


Nestlé USA Issues Recall Of Limited Amounts Of Häagen-Dazs® Chocolate Chocolate Chip Ice Cream In East Coast Region Due To Mismatched Packaging

Ice Cream Contains Peanuts Not Identified on Bottom Carton

FOR IMMEDIATE RELEASE - June 27, 2014 - Nestlé USA is initiating a recall of limited amounts of ice cream due to mismatched packaging. The affected products are 14-ounce cartons labeled as Häagen-Dazs Chocolate Chocolate Chip Ice Cream with a UPC of 74570-08400, and lid labeled as Häagen-Dazs Chocolate Peanut Butter. The best buy date and manufacturing code appear on the bottom of the carton: Best By date of 13May2015, Manufacturing code of 24-52 4133580418D.

These mismatched packages contain Chocolate Peanut Butter ice cream, and the ingredient statement on the carton applies to Chocolate Chocolate Chip Ice Cream and does not identify peanuts. People who have an allergy or severe sensitivity to peanuts may run the risk of serious or potentially life-threatening allergic reaction if they consume this product.

The ice cream was produced on May 13, 2014 and has been distributed in District of Columbia, Delaware, Florida, Maryland, North Carolina, New Jersey, New York, Pennsylvania, South Carolina, Virginia and West Virginia. No other production dates, sizes or varieties of Häagen-Dazs ice cream are affected by this recall. Häagen-Dazs product distributed in Canada is also not affected. Only products with mismatched flavor lids and cartons totaling 10,000 packages in the Eastern U.S. are being recalled.

A consumer reported the mismatched packaging to Nestlé. The company is investigating this incident and is working with the U.S. Food and Drug Administration in implementing this product recall. Nestlé is also working with Food Allergy Research & Education to alert consumers in the affected areas.

http://www.fda.gov/Safety/Recalls/ucm403194.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 1, 2014 3:32:50 AM


Health Matters America Inc. Of Cheektowaga, New York, Recalls Additional Sprouted Chia Seed And Sprouted Chia & Flax Seed Powder Due To Possible Health Risk

FOR IMMEDIATE RELEASE - June 26, 2014 - HEALTH MATTERS AMERICA INC. of Cheektowaga, New York is expanding the voluntary recall of Organic Traditions Sprouted Chia Seed Powder and Sprouted Chia& Flax Seed Powder due to possible Salmonella contamination, an organism that can cause serious and sometimes fatal infections in young children, elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses.

The recall is being expanded to include more lot numbers and other products that contain Chia Seeds. Health Matters America is committed to the safety of its customers.

These products have been distributed nationwide.

The products and lot numbers included in this voluntary recall have been expanded to include <click on the link below to view the recalled products>.

No other Organic Traditions products are affected by this recall.

http://www.fda.gov/Safety/Recalls/ucm403069.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jul 1, 2014 3:31:08 AM


Kraft Foods Group Voluntarily Recalls Small Quantity of Velveeta Original Pasteurized Recipe Cheese Product Due to Low Levels of Preservative Ingredient

FOR IMMEDIATE RELEASE - June 19, 2014- Kraft Foods Group is voluntarily recalling 260 cases of Velveeta Original Pasteurized Recipe Cheese Product because it does not contain appropriate levels of sorbic acid, a preservative ingredient. While unlikely, the affected product could spoil prematurely and/or lead to food borne illness. Therefore, the company is issuing this recall as a precaution.

This recall affects one batch of product made on one manufacturing line during a few hours of production. The product was shipped to three Walmart distribution centers and may have been redistributed to stores in up to 12 Midwest states. The affected products may have been shipped to Walmart stores in Colorado, Illinois, Indiana, Iowa, Kansas, Michigan, Minnesota, Nebraska, North Dakota, Ohio, South Dakota and Wisconsin. These products were not shipped outside of the U.S.

http://www.fda.gov/Safety/Recalls/ucm402337.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 26, 2014 6:49:48 AM


Recall Notification Report 040-2014 (Pork Products)

Class III Recall 040-2014

WASHINGTON, June 25, 2014 – Rudolph Foods, a Lawrenceville, Ga. establishment, is recalling approximately 34 pounds of pork products due to misbranding. The product contains monosodium glutamate (MSG), which is not declared on the label, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The product subject to recall includes:

1.75-oz. packages of “Lee’s Pig Skins Soft Style Cracklins” with a Sell By date of only “SEP 5 2014”

The bags, labeled as Lee’s Pig Skins Soft Style Cracklins, actually contain salt and vinegar cracklins that contains MSG as an ingredient.

The product, packaged June 3, 2014, bears the establishment number “EST-1425” within the Sell By code. The product was shipped to retail locations in Alabama, Georgia, Florida, Louisiana, Maryland and Mississippi.

The problem was discovered by a customer who opened a case and found salt and vinegar cracklins packaged in plain “Soft Style Cracklins” bags. It should be noted that MSG can cause a brief reaction in people with sensitivity to MSG. Anyone concerned about a reaction should contact a healthcare provider.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/rnr-040-2014

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 26, 2014 6:47:43 AM


Iowa Firm Recalls Sausage Products Containing Soy and Wheat Due to Misbranding and Undeclared Allergens

Class II Recall 039-2014
Health Risk: Low

WASHINGTON, June 25, 2014 – K & W Sausage, an Evansdale, Iowa, establishment, is recalling approximately 1,761 pounds of sausage products because of misbranding and undeclared allergens. The products contain soy and wheat, known allergens, which are not declared on the product labels.

The products subject to recall include:

16-oz. vacuum packed “Hot Franks” with a packaging code in the format “###14”

Various size packages of “Polish Sausage Hot” with packaging codes 15314, 15514, 16114, 16214, 16814, 16514, or 16914

Various size packages of “Beef Polish Sausage Hot” with packaging codes 15314, 15514, 16114, 16214, 16814, 16514, or 16914

The products subject to recall bear “EST. 15708” inside the USDA mark of inspection on the labels. The Hot Franks were produced on various dates from January 16, through June 20, 2014. The other products were produced on various dates from June 3, through June 18, 2014. All products were distributed to retailers in Iowa.

The mislabeling in the Polish sausage products occurred due to a change to using this ingredient. FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-039-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 22, 2014 7:45:09 AM


California Firm Recalls Pork Mini Buns Products Due to Misbranding and Undeclared Allergens

WASHINGTON, June 21, 2014– Wei-Chuan USA, Inc., a Bell Gardens, Calif., establishment, is recalling approximately 332 pounds of Pork Mini Buns Crab Meat Added due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products were formulated with fish, shellfish and egg, known allergens. However, the product was released with a label for Pork Mini Buns which does not declare fish, shellfish or egg.

The products were produced June 3, 2014 and have the product code “DF03A” printed on the bag. The products bear the establishment number “Est. 9034” inside the USDA mark of inspection. The products were sold to retail establishments in California.

FSIS and the company have received no reports of adverse reactions due to consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-038-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 22, 2014 7:40:43 AM


Michigan Firm Recalls Bacon Product Due To Misbranding and Undeclared Allergen

WASHINGTON, June 19, 2014– Dearborn Sausage Co., a Dearborn, Mich., establishment, is recalling approximately 3,660 pounds of slab bacon due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product was formulated with hydrolyzed soy protein, a known allergen, which is not declared on the product label.

The product was produced on March 11, April 4, and May 2, 2014.

FSIS and the company have received no reports of adverse reactions due to consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-037-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 22, 2014 7:36:43 AM


Ohio Firm Recalls Chicken Pad Thai Product Due to Misbranding and Undeclared Allergen

Class I Recall 036-2014
Health Risk: High

WASHINGTON, June 19, 2014– Bellisio Foods, Inc., a Jackson, Ohio, establishment, is recalling approximately 12,180 pounds of a Thai Kitchen Chicken Pad Thai frozen entrée product due to misbranding and an undeclared allergen, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains soy protein isolate, a known allergen, which is not declared on the product label.

The product was produced on April 8 and April 25, 2014. The product bears the establishment number “P-18297” inside the USDA mark of inspection. The product was distributed to retail stores nationwide.

The problem was discovered by the company when they conducted a label review and found that all the sub-ingredients of the Chicken Pad Thai were not listed on the packaging labels.

FSIS and the company have received no reports of adverse reactions due to consumption of these products.

http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2014/recall-036-2014-release

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 22, 2014 7:33:40 AM


Domega NY International Co Ltd Issues Allergy Alert On Undeclared Peanuts And Milk In Gong Xifacai Gift Chocolates

FOR IMMEDIATE RELEASE – June 17, 2014 – DOMEGA NY INTERNATIONAL CO LTD, 47-57 BRIDGEWATER STREET BROOKLYN NY 11222 is recalling Gong xiFacai gift chocolates because it contains undeclared peanuts and milk. Consumers who have allergies to peanuts and milk run the risk of serious or life-threatening allergic reactions if they consume this product.

The recalled Gong xiFacai gift chocolates comes in an un-coded, 238 gram plastic tray with a plastic overwrap package. It was sold in New York City. It is a product of China. The UPC code is 6 934169 900335.

No illnesses have been reported to date in connection with this product.

http://www.fda.gov/Safety/Recalls/ucm401564.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 17, 2014 7:15:05 AM


Wegmans Food Markets, Inc. Issues Allergy Alert on Undeclared Egg in Wegmans Cinnamon Raisin Buns, 12 oz.

FOR IMMEDIATE RELEASE - June 16, 2014 - Wegmans Food Markets, Inc. in Rochester, NY, has initiated a voluntary recall of approximately 1,315 units of Wegmans Cinnamon Raisin Buns, 12 oz., because they may contain egg, which is not declared on the label. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume this product. The finished product may also have been contaminated with raw egg; therefore, there is also the potential for an unknown pathogen that may cause illness if consumed.

Wegmans Cinnamon Raisin Buns are produced by Wegmans Central Bakeshop and sold exclusively in 84 Wegmans stores located in New York, Pennsylvania, New Jersey, Massachusetts, Virginia and Maryland.

Wegmans Cinnamon Raisin Buns have a white frosting and are sold in the bakery department. The product is packaged in a clear plastic clamshell and bears UPC 77890 92218, and Use-by-Date of 6/19/14 only (stamped on top of package).

There have been no reported injuries or illnesses to date associated with this recall.

http://www.fda.gov/Safety/Recalls/ucm401323.htm

Profile Pic
hawaii5oh
Champion Author Honolulu

Posts:18,897
Points:2,636,195
Joined:May 2007
Message Posted: Jun 17, 2014 7:13:42 AM


Schnucks Bakery Recalls Devil’s Food Cakes Topped With Undeclared Pecans

FOR IMMEDIATE RELEASE – June 13, 2014 – Schnucks Bakery has issued a voluntary recall on Devil’s Food Cakes decorated with pecans. Anyone with a pecan allergy who consumed this product may be at risk for serious reaction.

During an ingredient/label review, it was noted that although pecans were visible on top of the cake (not baked inside), the known allergen was not disclosed on the label.

These cakes were sold at all Schnucks stores in Missouri, Illinois, Indiana, Iowa and Wisconsin. If you have a pecan allergy and have purchased the Schnucks Devil’s Food Cake, you may return it to any Schnucks store:

There have been no reports of illness associated with this recall. However, if you are concerned about a possible allergic reaction please contact your physician.

http://www.fda.gov/Safety/Recalls/ucm401227.htm

Post a reply Back to Topics