Summary Company Announcement Date: June 03, 2024 FDA Publish Date: June 03, 2024 Product Type: Food & Beverages Spices, Flavors & Salts Foodborne Illness Reason for Announcement: Recall Reason Description Potential Contamination with Salmonella Company Name: UBC Food Distributors Brand Name: Brand Name(s) Product Description: Product Description Ground black pepper Company Announcement UBC Food Distributors in…
Fresh Start Produce Sales Initiates Recall of Whole Cucumbers Because of Possible Health Risk
Summary Company Announcement Date: May 31, 2024 FDA Publish Date: June 01, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Salmonella Company Name: Fresh Start Produce Sales, Inc. Brand Name: Brand Name(s) No Brand Name Product Description: Product Description Whole Cucumbers Company Announcement FOR IMMEDIATE RELEASE- May 31, 2024 – Fresh…
Medline Industries, LP Issues Nationwide Recall of SubG Endotracheal Tube with Subglottic Suction
Summary Company Announcement Date: May 31, 2024 FDA Publish Date: May 31, 2024 Product Type: Medical Devices Reason for Announcement: Recall Reason Description The inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, loss of pressure, or inability to inflate. Company Name: Medline Industries LP…
Biloxi Restaurant and its Co-Owner Plead Guilty to Conspiracy to Misbrand Seafood
Department of JusticeU.S. Attorney’s OfficeSouthern District of Mississippi FOR IMMEDIATE RELEASEThursday, May 30, 2024 Gulfport, MS – A Mississippi corporation operating as Mary Mahoney’s Old French House restaurant in Biloxi, Mississippi, pled guilty today to conspiracy to misbrand seafood and wire fraud. A co-owner/manager of the restaurant also pled guilty to misbranding of seafood. According…
OptumHealth Care Solutions Recalls Nimbus II Infusion Pump Systems Under Recall by InfuTronix, LLC
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….