Food Recalls Archives - Page 1245 of 1297

Stryker Craniomaxillofacial Issues Nationwide Recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile (December 23)

January 1, 2009 By The FDA Leave a Comment

Stryker Craniomaxillofacial has issued a nationwide recall of its Custom Cranial Implant Kits; Catalogue Numbers 54-00101, 54-00102, 54-00103 and 54-00104, all lots shipped sterile Stryker's Craniomaxillofacial (CMF) business unit announced today that the U.S. Food and Drug Administration (FDA) concluded on Dec. 18, 2008 that its recall of the … [Read more...]

Denver Burrito Recall – Listeria Contamination

December 31, 2008 By The USDA Leave a Comment

Recall Release CLASS I RECALL FSIS-RC-053-2008 HEALTH RISK: HIGH Congressional and Public Affairs (202) 720-9113 Roger Sockman WASHINGTON, Dec. 30, 2008 - Home Fresh Sandwich Distributors, Inc., a Denver, Colo., firm, is recalling approximately 172 pounds of burrito products that may be contaminated with Listeria monocytogenes, the U.S. … [Read more...]

Missouri Firm Recalls Sausage Products For Possible Listeria Contamination

December 26, 2008 By The USDA Leave a Comment

Recall Release CLASS I RECALL FSIS-RC-052-2008 HEALTH RISK: HIGH Congressional and Public Affairs (202) 720-9113 Peggy Riek WASHINGTON, Dec. 25, 2008 - T. Piekutowski European Style Sausage, a St. Louis, Mo., firm, is recalling approximately 750 pounds of sausage products that may be contaminated with Listeria monocytogenes, the U.S. … [Read more...]

KRC Food Trading Inc. Recall of Fish Cake Sushi

December 25, 2008 By The FDA Leave a Comment

CONTACT: MS JOANNA KIM 1-213-388-8215 FOR IMMEDIATE RELEASE DECEMBER 23, 2008--LOS ANGELES, CA--KRC FOOD TRADING INC IS RECALLING ITS FISH CAKE SUSHI WITH PRODUCTION DATE OF DECEMBER 19 AND DECEMBER 22 DUE TO THE LABEL NOT DECLARING EGGS. PEOPLE WHO HAVE AN ALLERGY OR SEVERE SENSITIVITY TO EGGS RUN THE RISK OF SERIOUS OR LIFE-THREATENINGALLERGIC … [Read more...]

KV Pharmaceutical Suspends Shipments on All Drugs in Pill Form Including Hydromorphone

December 24, 2008 By The FDA 1 Comment

Note: Also see related ETHEX Hydromorphone Recall CONTACT: CATHERINE BIFFIGNANI (314) 645-6600 FOR IMMEDIATE RELEASE --ST. LOUIS – DEC. 23, 2008 – KV PHARMACEUTICAL HAS ADVISED THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) THAT, EFFECTIVE MIDNIGHT DEC. 19, 2008, THE COMPANY VOLUNTARILY SUSPENDED ALL SHIPMENTS OF ALL FDA APPROVED DRUG PRODUCTS IN … [Read more...]