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 Name: Optum Nimbus II Plus Ambulatory Infusion System Product Codes: See Recall Database entry Distribution Dates: August 19, 2020 to April 20, 2024 Devices Recalled in…
Tea Woman Sentenced for Obtaining a Controlled Substance by Fraud
Department of JusticeU.S. Attorney’s OfficeDistrict of South Dakota FOR IMMEDIATE RELEASETuesday, May 28, 2024 SIOUX FALLS – United States Attorney Alison J. Ramsdell announced today that U.S. District Judge Karen E. Schreier has sentenced a Tea, South Dakota, woman convicted of Obtaining a Controlled Substance by Misrepresentation, Fraud, Forgery, Deception, and Subterfuge. The sentencing took…
Sagent Pharmaceuticals Issues Voluntary Nationwide Recall of Docetaxel Injection, USP Due to Potential Presence of Particulate Matter
Summary Company Announcement Date: May 28, 2024 FDA Publish Date: May 29, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Potential presence of particulate matter Company Name: Sagent Pharmaceuticals Brand Name: Brand Name(s) Product Description: Product Description Docetaxel Injection, USP Company Announcement FOR IMMEDIATE RELEASE – SCHAUMBURG, IL – May 28, 2024 –…
Dairy Manufacturers Inc. Issues Voluntary Recall of Products Due to Non-Compliance with Requirements Under the 21 CFR 106.110 New Infant Formula Registration
Summary Company Announcement Date: May 24, 2024 FDA Publish Date: May 25, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Food Compliance Programs – Baby Formula Company Name: Dairy Manufacturers Inc. Brand Name: Brand Name(s) Crecelac and Farmalac Product Description: Product Description Infant Formula Company Announcement Dairy Manufacturers Inc., of Prosper,…
Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices
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. Please be aware, this recall is a correction, not a product removal. Recalled Product Product Names: BioZorb Marker Product Codes: NEU Model Numbers: F0405 BioZorb Marker 4cm x…
AMB Food Inc. Issues Allergy Alert on Undeclared Wheat in Product
Summary Company Announcement Date: May 23, 2024 FDA Publish Date: May 24, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared allergen – wheat Company Name: AMB Food Inc Brand Name: Brand Name(s) Pop a Nosh Product Description: Product Description Mixed Munch Regular and Honey BBQ Company Announcement AMB Food Inc….
Vyaire Medical, Inc. Recalls the Twin Tube Due to The Potential of The Nozzle Separating During Patient Use
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: Twin Tube Product Codes: BZC Model Numbers: V-707327 Distribution Dates: January 1, 2015 to June 30, 2023 Devices Recalled in the U.S.: 649 Date Initiated…
County Road Seafood Issues Allergy Alert of Undeclared Egg in 4 Oz Packages of County Road Seafood Crab Cake
Summary Company Announcement Date: May 21, 2024 FDA Publish Date: May 22, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Egg Company Name: County Road Seafood Inc. Brand Name: Brand Name(s) County Road Seafood Product Description: Product Description Crab Cake 2 Pack Company Announcement County Road…
World Green Nutrition, Inc. Expands Recall of Tejocote Products Due to the Presence of Yellow Oleander
Summary Company Announcement Date: May 21, 2024 FDA Publish Date: May 21, 2024 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Product contains yellow oleander Company Name: World Green Nutrition, Inc. Brand Name: Brand Name(s) Green ELV Nutrition Product Description: Product Description Elv Control Herbal Supplement Company Announcement World Green…
Hospira Inc. Issues A Voluntary Nationwide Recall For Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units Due to the Potential for Incomplete Crimp Seals
Summary Company Announcement Date: May 21, 2024 FDA Publish Date: May 22, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Packaging Defect Company Name: Hospira Inc. Brand Name: Brand Name(s) Product Description: Product Description Buprenorphine Hydrochloride Injection Carpuject Units and Labetalol Hydrochloride Injection, USP Carpuject Units Company…