This recall involves correcting certain devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without correction. Affected Product Product Names: Plum Duo Infusion System…
Aquastar (USA) Corp Recalls Kroger Mercado Frozen Cooked Shrimp Because of Possible Health Risk
Summary Company Announcement Date: August 27, 2025 FDA Publish Date: August 28, 2025 Product Type: Food & Beverages Shellfish Contaminants Reason for Announcement: Recall Reason Description Potential Contaminant – cesium-137 (Cs-137) Company Name: Aquastar Corp Brand Name: Brand Name(s) Product Description: Product Description Mercado Frozen Cooked Shrimp Company Announcement August 27, 2025, AquaStar (USA) Corp…
Aquastar (USA) Corp Recalls Cocktail Shrimp 6oz Because of Possible Health Risk
Summary Company Announcement Date: August 28, 2025 FDA Publish Date: August 28, 2025 Product Type: Food & Beverages Shellfish Contaminants Reason for Announcement: Recall Reason Description Potential Contaminant – cesium-137 (Cs-137) Company Name: Aquastar Corp Brand Name: Brand Name(s) Product Description: Product Description Cocktail Shrimp Company Announcement August 28, 2025, AquaStar (USA) Corp of Seattle,…
Unichem Pharmaceuticals (USA) Inc. Issues Voluntary Nationwide Recall of Cyclobenzaprine Hydrochloride Tablets USP 10 mg, Due to Mislabeling
Summary Company Announcement Date: August 27, 2025 FDA Publish Date: August 27, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Device & Drug Safety – Mislabel Company Name: Unichem Pharmaceuticals Brand Name: Brand Name(s) Unichem Pharmaceuticals Product Description: Product Description Cyclobenzaprine Hydrochloride Tablets USP 10 mg Company Announcement FOR IMMEDIATE RELEASE – 08/27/2025–…
Viva Raw Issues Voluntary Recall of Two Lots of Dog and Cat Foods Due to Salmonella and Listeria Monocytogenes Contamination
Summary Company Announcement Date: August 25, 2025 FDA Publish Date: August 25, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella and Listeria monocytogenes contamination Company Name: Viva Raw LLC. Brand Name: Brand Name(s) Product Description: Product Description Ground Beef for Dogs and Ground Chicken for Dogs and Cats…
Country Eggs, LLC Recalls Large Brown Cage Free “Sunshine Yolks” Because of Possible Health Risk
Summary Company Announcement Date: August 27, 2025 FDA Publish Date: August 27, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Country Eggs, LLC Brand Name: Brand Name(s) Country Eggs, NIJIYA, GOLDEN YOLK Product Description: Product Description Large Brown Cage Free Eggs Company…
Company Voluntarily Recalls Honey Balsamic Salad Kit Due to Potential Undeclared Sesame and Soy
Summary Company Announcement Date: August 26, 2025 FDA Publish Date: August 26, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Allergen – Sesame and Soy Company Name: Taylor Fresh Foods Brand Name: Brand Name(s) Taylor Farms Product Description: Product Description Honey Balsamic Salad Kit Company Announcement Salinas, Calif., August…
Viva Raw Issues Voluntary Recall of Two Lots of Dog an Cat Foods Due to Salmonella and Listeria Monocytogenes Contamination
Summary Company Announcement Date: August 25, 2025 FDA Publish Date: August 25, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella and Listeria monocytogenes contamination Company Name: Viva Raw LLC. Brand Name: Brand Name(s) Product Description: Product Description Ground Beef for Dogs and Ground Chicken for Dogs and Cats…
FDA Update on the Safety of Ixchiq (Chikungunya Vaccine, Live). FDA Suspends Biologics License: FDA Safety Communication
AUDIENCE: Patient, Health Care Professional, Pharmacy, Cardiology, Neurology, Internal Medicine, Family Practice, Travel Clinics UPDATE: On August 22, 2025, the US FDA’s Center for Biologics Evaluation and Research (CBER) has suspended the biologics license for Valneva Austria GmbH’s Ixchiq (Chikungunya Vaccine, Live). This vaccine was initially approved by FDA under the accelerated approval pathway in…
Follow Instructions for Safe Use of Hyperbaric Oxygen Therapy Devices – Letter to Health Care Providers
August 25, 2025 The U.S. Food and Drug Administration (FDA) is reminding health care providers and facilities about the safe use of hyperbaric oxygen therapy (HBOT) devices and the importance of following the manufacturer’s instructions for use. The FDA is aware of reports of serious injuries and deaths with use of HBOT devices and is…