Food Recalls Archives - Page 375 of 1293

Amneal Pharmaceuticals, LLC. Issues Voluntary Nationwide Recall of Ranitidine Tablets, USP, 150mg and 300mg, and Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity

November 12, 2019 By The FDA Leave a Comment

Description Lot# Expiration Date Ranitidine Tablets, USP 150mg AR180483B 3/31/2020 Ranitidine Tablets, USP 150mg AR180559A 3/31/2020 Ranitidine Tablets, USP 150mg AR180560A 3/31/2020 Ranitidine Tablets, USP 150mg AR180594A 3/31/2020 Ranitidine Tablets, USP 150mg AR180595A 3/31/2020 Ranitidine Tablets, USP … [Read more...]

Taher Voluntarily Recalls Veggie & Ranch Cups With Cauliflower Because of Possible Health Risk

November 12, 2019 By The FDA Leave a Comment

Summary Company Announcement Date: November 11, 2019 FDA Publish Date: November 11, 2019 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Due to the potential risk of Listeria monocytogenes Company Name: Taher, Inc. Brand Name: Brand Name(s) Fresh Seasons Kitchen Product Description: Product … [Read more...]

Ezzo Sausage Company Recalls Meat Products due to Possible Listeria Contamination

November 9, 2019 By The USDA Leave a Comment

WASHINGTON, Nov. 9, 2019 – Ezzo Sausage Company, a Columbus, Ohio establishment, is recalling approximately 25,115 pounds of sausage products that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The ready-to-eat sausage products were produced … [Read more...]

Russ Davis Wholesale Voluntarily Recalling Products Due to Possible Health Risk

November 8, 2019 By The FDA Leave a Comment

Summary Company Announcement Date: November 08, 2019 FDA Publish Date: November 08, 2019 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: Russ Davis Wholesale Brand Name: Brand Name(s) Crazy Fresh, quick & easy, no brand name listed Product … [Read more...]

Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared Sildenafil

November 8, 2019 By The FDA Leave a Comment

Summary Company Announcement Date: November 08, 2019 FDA Publish Date: November 08, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Product is tainted with sildenafil Company Name: Med Man Distribution Brand Name: Brand Name(s) Product Description: Product Description Up2 THERE IS NO OTHER All Natural Libido … [Read more...]