The recall described in this notice is for the same issue that was announced in Do Not Use Certain Mighty Bliss Electric Heating Pads Due to Risk of Injury: FDA Safety Communication | FDA on October 25, 2022. The FDA has identified this as a Class I recall, the most serious type of recall. Use…
Wegmans Food Markets, Inc. Announces Voluntary Recall of Products Containing Micro Greens, Sweet Pea Leaves, and Cat Grass Because of Possible Health Risk
Summary Company Announcement Date: December 23, 2022 FDA Publish Date: December 23, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential presence of Salmonella Company Name: Wegmans Food Markets, Inc. Brand Name: Brand Name(s) Wegmans Organic Product Description: Product Description Microgreens, sweet pea leaves, cat grass Company Announcement ROCHESTER, NY –…
World Variety Produce, Inc. Voluntarily Recalls Melissa’s Pasta Para Duros 12oz Because it Contains Undeclared Wheat Allergens
Summary Company Announcement Date: December 23, 2022 FDA Publish Date: December 23, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Wheat Company Name: World Variety Produce, Inc. Brand Name: Brand Name(s) Melissa’s Product Description: Product Description Pasta Para Duros Company Announcement People with an allergy or severe sensitivity to Wheat…
Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam Adhesion Failure and Residual PE‐PUR Foam Debris: FDA Safety Communication
Date Issued: December 22, 2022 The U.S. Food and Drug Administration (FDA) is providing additional information to patients, caregivers, and health care providers about two recent issues in certain reworked Philips Respironics (Philips) Trilogy 100 and Trilogy 200 ventilators. These Philips Trilogy 100 and Trilogy 200 ventilators were recalled in June 2021 for issues with…
Meijer Announces Allergy Alert on Undeclared Almonds in True Goodness Oat-Based Plain Yogurt Alternative
Summary Company Announcement Date: December 16, 2022 FDA Publish Date: December 22, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Tree Nuts Company Name: Meijer Brand Name: Brand Name(s) True Goodness Product Description: Product Description Plain Yogurt Alternative Company Announcement Summary of Recall: Culture Fresh Foods is issuing a recall…
Alpha Foods Issues a Product Recall Due to Undeclared Milk in Meatless Burritos & Breakfast Sandwiches
Summary Company Announcement Date: December 21, 2022 FDA Publish Date: December 21, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Milk Company Name: The Miso Brothers Inc Brand Name: Brand Name(s) Product Description: Product Description Frozen Burritos Company Announcement Alpha Foods, Glendale, California (December 21, 2022) – Out of an…
Lupin Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Four Lots of Quinapril Tablets Due to Potential Presence of N-Nitroso-Quinapril Impurity
Summary Company Announcement Date: December 21, 2022 FDA Publish Date: December 21, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of nitrosamine impurity, N-Nitroso-Quinapril Company Name: Lupin Pharmaceuticals Inc. Brand Name: Brand Name(s) Product Description: Product Description Quinapril 20 and 40 mg tablets Company Announcement Baltimore, Maryland, December 21, 2022: Lupin Pharmaceuticals…
Falcon Import and Export, LLC Issues Allergy Alert on Undeclared Milk & Wheat in Mixed Alsultan Branded Baklava, and Undeclared Cashews, Pistachios, & Almonds in Alsultan Branded Betefour
Summary Company Announcement Date: December 20, 2022 FDA Publish Date: December 20, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Milk and Tree Nuts Company Name: Falcon Import and Export LLC Brand Name: Brand Name(s) Product Description: Product Description Baklava and Betefour Company Announcement Falcon Import and Export LLC, of…
Arrow International, LLC, subsidiary of Teleflex, Inc Recalls Arrow AutoCAT 2, AC3 Intra-Aortic Balloon Pumps for Unexpectedly Short Battery Run Times
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: Arrow AutoCAT 2, AutoCAT 2 Refurbished, AeroautoCAT 2, AutoCAT 2 Wave, AutoCAT 2 Wave refurbished, AeroautoCAT 2 Wave, AeroautoCAT 2 Wave refurbished, AC3 NA/EMEA, AC3…
Former Registered Nurse Charged with Tampering with Medical Grade Fentanyl
Department of JusticeSouthern District of Florida FOR IMMEDIATE RELEASEFriday, December 16, 2022 MIAMI – A South Florida federal grand jury has charged Martin County resident Catherine Shannon Dunton, 54, with tampering with vials of liquid fentanyl at an outpatient surgery center where she worked as a licensed registered nurse. Medical providers use a liquid form of…