Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 07, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: Raja Foods LLC Brand Name: Brand Name(s) Product Description: Product Description Cinnamon Powder Company Announcement Raja Foods LLC of Skokie, Il is recalling its…
Expanded Press Release – Kalo Foods, LLC Recalls Single Slice Carrot Cake and Chocolate Cake Due to Undeclared Soy Allergen
Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 08, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Soy Company Name: KALO Foods, LLC Brand Name: Brand Name(s) Product Description: Product Description Single Slices of Carrot Cake & Chocolate Cake Company Announcement KALO Foods,…
Stonewall Kitchen Issues Allergy Alert for Wheat in Limited Quantity of Gluten Free Cinnamon Sugar Doughnut Mix
Summary Company Announcement Date: March 07, 2024 FDA Publish Date: March 07, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Wheat Company Name: Stonewall Kitchen Brand Name: Brand Name(s) Stonewall Kitchen Product Description: Product Description Gluten Free Cinnamon Sugar Doughnut Mix Company Announcement Stonewall Kitchen of…
Medtronic Neurosurgery Recalls Duet External Drainage and Monitoring System Catheter Tubing due to a Potential for the Catheter Disconnection from the Patient Line Stopcock Connectors
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: Medtronic Duet External Drainage and Monitoring System Catheter Tubing Product Codes: PCB Class 1 Device Recall Medtronic Duet External Drainage and Monitoring System, SmartSite Injection…
Aji Mori Sauce Corp. DBA Sushi Koo Issues Voluntary Recall of Chillimami Sauce
Summary Company Announcement Date: February 29, 2024 FDA Publish Date: March 06, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Clostridium botulinum Company Name: AJI MORI Sauce Corp. DBA Susi Koo Brand Name: Brand Name(s) Product Description: Product Description CHILLIMAMI SAUCE Company Announcement Product -Recall Important Information…
Colonna Brothers, Inc. Issues a Voluntary Recall for “1.5oz Marcum Ground Cinnamon & 2.25oz Supreme Tradition Ground Cinnamon” Because of Possible Health Risk Due to Elevated Lead Levels
Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 06, 2024 Product Type: Food & Beverages Spices, Flavors & Salts Contaminants Reason for Announcement: Recall Reason Description Elevated Lead Levels Company Name: Colonna Brothers, Inc. Brand Name: Brand Name(s) Product Description: Product Description Marcum Ground Cinnamon & Supreme Tradition Ground Cinnamon Company Announcement FOR…
El Chilar Rodriguez LLC. Issues Voluntary Recall of El Chilar Ground Cinnamon “Canela Molida” Due to Elevated Lead Levels
Summary Company Announcement Date: March 06, 2024 FDA Publish Date: March 06, 2024 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Metal Contaminant – Lead Company Name: El Chilar Rodriguez LLC Brand Name: Brand Name(s) Product Description: Product Description Ground Cinnamon “Canela Molida” Company Announcement El Chilar Rodriguez LLC of Apopka,…
Houma Doctor Pleads Guilty to Distributing Misbranded Versions of Injectable Contraceptives to Patients
Department of JusticeU.S. Attorney’s OfficeEastern District of Louisiana FOR IMMEDIATE RELEASETuesday, March 5, 2024 NEW ORLEANS – U.S. Attorney Duane A. Evans announced today that MICHELLE ANDRE, a resident and doctor in Houma pled guilty to a one-count bill of information on February 29, 2024 before United States District Judge Barry Ashe, to distributing misbranded drugs…
Generic Pharmaceuticals Manufacturer Pleads Guilty, Agrees to $1.5 Million Criminal Penalty for Distributing Adulterated Drugs and $2 Million to Resolve Civil Liability under the False Claims Act
Department of JusticeU.S. Attorney’s OfficeOffice of Public Affairs FOR IMMEDIATE RELEASEWednesday, March 6, 2024 KVK Research Inc., a generic drug manufacturer in Bucks County, Pennsylvania, pleaded guilty today to criminal charges that it introduced adulterated drugs into interstate commerce. A criminal information filed in federal court in Philadelphia charged KVK Research and its corporate affiliate, KVK…
Baxter Healthcare Recalls ExactaMix Pro 1200 and Pro 2400 Due to a Software Error
Please be aware, this recall is a correction, not a product removal. 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: ExactaMix Pro 1200, ExactaMix Pro 2400 Product Codes: LHI Model Numbers: ExactaMix Pro…