Summary Company Announcement Date: October 22, 2019 FDA Publish Date: October 22, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Contains Tadalafil Company Name: GL Holdings Brand Name: Brand Name(s) Green Lumber Product Description: Product Description Dietary supplements for male sexual enhancement Company Announcement FOR IMMEDIATE RELEASE – Newport Beach, California. GL Holdings…
Mylan Pharmaceuticals Initiates Voluntary Nationwide Recall of One Lot of Alprazolam Tablets, USP C-IV 0.5 mg, Due to the Potential of Foreign Substance
Summary Company Announcement Date: October 25, 2019 FDA Publish Date: October 26, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential presence of foreign substance Company Name: Mylan Pharmaceuticals Inc. Brand Name: Brand Name(s) Mylan Pharmaceuticals Inc. Product Description: Product Description Alprazolam Tablets, USP C-IV 0.5 mg Company Announcement Mylan Pharmaceuticals Inc. is…
Novitium Pharma Issues Voluntary National Recall of Ranitidine Hydrochloride Capsules 150mg and 300mg Due to an Elevated Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA)
Summary Company Announcement Date: October 25, 2019 FDA Publish Date: October 25, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description May contain N-Nitrosodimethylamine (NDMA) Company Name: Novitium Pharma Brand Name: Brand Name(s) Novitium Pharma Product Description: Product Description Ranitidine Hydrochloride Capsules 150 mg and 300 mg Company Announcement Novitium Pharma LLC (Novitium) is…
Sanofi Provides Update on Precautionary Voluntary Recall of Zantac OTC in U.S.
Summary Company Announcement Date: October 22, 2019 FDA Publish Date: October 23, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description May Contain N-Nitrosodimethylamine (NDMA) Company Name: Sanofi Brand Name: Brand Name(s) Product Description: Product Description Zantac 150, Zantac 150 Cool Mint, Zantac 75 (OTC Products) Company Announcement As a precautionary measure, Sanofi on…
Perrigo Company plc Issues Voluntary Worldwide Recall of Ranitidine Due to Possible Presence of Impurity, N-nitrosodimethylamine (NDMA) Impurity in the Product
Summary Company Announcement Date: October 23, 2019 FDA Publish Date: October 23, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of N-Nitrosodimethylamine (NDMA) Company Name: Perrigo Company plc Brand Name: Brand Name(s) Perrigo Company plc Product Description: Product Description Ranitidine (all pack sizes) Company Announcement As a precautionary measure, Perrigo Company plc…
Dr. Reddy’s Confirms its Voluntary Nationwide Recall of All Ranitidine Products in the U.S. Market
Summary Company Announcement Date: October 23, 2019 FDA Publish Date: October 23, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Contains N-Nitrosodimethylamine (NDMA) Company Name: Dr. Reddy’s Laboratories Ltd. Brand Name: Brand Name(s) Dr. Reddy’s, Kroger, Walgreens, and others Product Description: Product Description Ranitidine Tablets & Capsules Company Announcement Dr. Reddy’s Laboratories Ltd….
What to Know About Breast Implants
Should I get breast implants? Should they be saline or silicone? Which style? How much monitoring is needed after surgery? Those are common questions people have when considering breast implants. That’s why the U.S. Food and Drug Administration offers the following information to help people making decisions about breast implants. Breast implants are medical devices…
Good Dog, Bad Food: Foods for People That Are Bad for Your Dog
Español If you consider the family dog, well, family—and are apt to toss him a piece of your food now and then—proceed with caution. Some foods meant for human consumption can be dangerous, and even deadly, to your dog. How are people and animals different when it comes to food? According to Carmela Stamper, D.V.M.,…
Fitoterapia USA Inc. Issues Voluntary Nationwide Recall of MERO MACHO ARTIFICIAL PASSION FRUIT FLAVORED VITAMIN C LIQUID SUPPLEMENT Due to Presence of Active Ingredient Tadalafil
Summary Company Announcement Date: September 16, 2019 FDA Publish Date: September 16, 2019 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Tadalafil Company Name: Fitoterapia USA Inc. Brand Name: Brand Name(s) Product Description: Product Description MACHO ARTIFICIAL PASSION FRUIT FLAVORED VITAMIN C LIQUID SUPPLEMENT Company Announcement Fitoterapia USA Inc., is voluntarily recalling 19,000…
Teleflex Medical Recalls the Hudson RCI Sheridan and Sheridan Endotracheal Tubes Due to Risk of the Sheridan Connector Disconnecting from the Breathing Circuit
Hudson RCI® Sheridan LTS® 4.0 mm Hudson RCI® Sheridan® Preformed 3.0 mm Hudson RCI® Sheridan LTS® 5.0 mm Hudson RCI® Sheridan® Preformed 3.5 mm Hudson RCI® Sheridan LTS® 6.0 mm Hudson RCI® Sheridan® Preformed 4.0 mm Hudson RCI® Sheridan/CF® 3.0 mm Hudson RCI® Sheridan® Preformed 4.5 mm Hudson RCI® Sheridan/CF® 3.5 mm Hudson RCI® Sheridan®…