Food Recalls Archives - Page 490 of 1297

Supermercado Selectos Recalls Raw, Frozen Meat and Poultry Products Produced Without Benefit of Inspection

June 1, 2018 By The USDA Leave a Comment

WASHINGTON, June. 1, 2018 – Supermercado Selectos, a San Sebastián, Puerto Rico firm, is recalling an undetermined amount of various raw, frozen beef, pork and poultry products that were produced without the benefit of federal inspection, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced … [Read more...]

SDQ Trading Inc Issues Alert on Undeclared Milk Allergen in Cheese Biscuits

June 1, 2018 By The FDA Leave a Comment

SDQ Trading Inc. of 651A Lexington Ave, Brooklyn, NY 11221 is recalling its 16.5 oz packages of Cheese Biscuits because they may contain undeclared milk allergen. Consumers who are allergic to milk allergen may run the risk of serious or life-threatening allergic reactions if they consume this product. The recalled Cheese Biscuits were distributed … [Read more...]

SunMed Holdings, LLC Issues a Nationwide Recall of STAT-Check and Medline Manual Resuscitator Bags

June 1, 2018 By The FDA Leave a Comment

On May 29, 2018, SunMed Holdings, LLC initiated a nationwide recall of 18,808 units of STAT-Check and Medline resuscitator bags which were distributed between February 1, 2018 to May 13, 2018. The patient port retaining ring of the affected bags may not fully seat which may allow the patient port to detach during use. If this takes place, the … [Read more...]

Eddy Packing Co., Inc. Recalls Smoked Sausage Product due to Possible Foreign Matter Contamination

May 31, 2018 By The USDA Leave a Comment

WASHINGTON, MAY 31, 2018 – Eddy Packing Co., Inc., a Yoakum, Texas establishment, is recalling approximately 18,390 pounds of smoked sausage that may be contaminated with extraneous materials, specifically soft plastic, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.The frozen, … [Read more...]

Abbott Implements Corrective Action for Heartmate 3 Heart Pump

May 31, 2018 By The FDA Leave a Comment

Abbott is communicating to physicians about a field corrective action related to the HeartMate 3™ Left Ventricular Assist Device (LVAD). Abbott notified physicians and global regulatory bodies on April 5, 2018, that outflow graft twisting could occur post-implant in the HeartMate 3 LVAD, resulting in a persistent low flow alarm that may … [Read more...]