FDA Press Releases Archives - Page 348 of 815

Mavidon Issues Voluntary Worldwide Recall of Manufactured Products Including Lemonprep® Tubes And Single Use Cups Pediaprep® Tubes And Single Use Cups Wave Prep® Tubes And Single Use Cups Cardio Prep Single Use Cups Due To Burkholderia Cepacia Contamination

January 8, 2020 By The FDA Leave a Comment

Summary Company Announcement Date: December 23, 2019 FDA Publish Date: January 08, 2020 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Burkholderia cepacia Company Name: Mavidon Brand Name: Brand Name(s) LemonPrep®, PediaPrep®, Wave Prep, Cardio Prep Product Description: Product … [Read more...]

Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity

January 8, 2020 By The FDA Leave a Comment

Summary Company Announcement Date: January 06, 2020 FDA Publish Date: January 08, 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) impurity Company Name: Denton Pharma, Inc. dba Northwind Pharmaceuticals Brand Name: Brand Name(s) Product Description: Product Description Ranitidine … [Read more...]

Fresh Location Announces Product Recall Due to Possible Listeria Contamination

January 8, 2020 By The FDA Leave a Comment

Summary Company Announcement Date: January 07, 2020 FDA Publish Date: January 08, 2020 Product Type: Food & BeveragesSnack Food ItemFoodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: Fresh Location Brand Name: Brand Name(s) Fresh Location Product … [Read more...]

Mylan Initiates Voluntary Nationwide Recall of Three Lots of Nizatidine Capsules, USP, Due to the Detection of Trace Amounts of NDMA (N-Nitrosodimethylamine) Impurity Found in the Active Pharmaceutical Ingredient Manufactured by Solara Active Pharma Sciences Limited

January 8, 2020 By The FDA Leave a Comment

Summary Company Announcement Date: January 08, 2020 FDA Publish Date: January 08, 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description NDMA (Nitrosodimethylamine) impurity Company Name: Mylan N.V. Brand Name: Brand Name(s) Product Description: Product Description Nizatidine Capsules 150mg and 300mg Company … [Read more...]

Lipari Foods Issues Recall of Various Wedge Deli Sandwiches Due to Potential Contamination of Listeria Monocytogenes

January 7, 2020 By The FDA Leave a Comment

Summary Company Announcement Date: January 06, 2020 FDA Publish Date: January 06, 2020 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria monocytogenes Company Name: Lipari Foods, LLC Brand Name: Brand Name(s) Premo, Fresh Grab Product Description: Product … [Read more...]