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...]
Russ Davis Wholesale Voluntarily Recalling Products Due to Possible Health Risk
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
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...]
American Health Packaging Issues Voluntary Nationwide Recall of Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups Due to the Detection of N-nitrosodimethylamine (NDMA) Impurity
Summary Company Announcement Date: November 08, 2019 FDA Publish Date: November 08, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) impurity Company Name: American Health Packaging Brand Name: Brand Name(s) Product Description: Product Description Ranitidine Liquid Unit Dose … [Read more...]
Aurobindo Pharma USA, Inc. Initiates Voluntary Nationwide Consumer Level Recall of 38 Lots of Ranitidine Tablets 150mg, Ranitidine Capsules 150mg, Ranitidine Capsules 300mg and Ranitidine Syrup 15mg/mL Due to the Detection of NDMA (Nitrosodimethylamine) Impurity
Summary Company Announcement Date: November 06, 2019 FDA Publish Date: November 06, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) Company Name: Aurobindo Pharma USA, Inc. Brand Name: Brand Name(s) Aurobindo & DG Health Product Description: Product … [Read more...]
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