Raja Foods Skokie, IL Is Recalling “Swad Brand Cinnamon Powder 3.5OZ Retail Packs” for Possible Lead Contamination

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,…

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…