This recall involves updating instructions for using devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it without following the updated instructions. Affected Product Product…
CHS Inc. Recalls Payback Champion Lamb Feed Due to Elevated Copper Health Risk
Summary Company Announcement Date: July 08, 2025 FDA Publish Date: July 09, 2025 Product Type: Animal & VeterinaryFood & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Elevated levels of copper Company Name: CHS, Inc. Brand Name: Brand Name(s) Product Description: Product Description Champion Lamb Text B30 with Power Booster Company Announcement CHS Inc….
Natureen International Inc. Recalls Wei-Chuan Dried Black Fungus Slice (2.5oz) Because of Possible Health Risk
Summary Company Announcement Date: July 08, 2025 FDA Publish Date: July 09, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Salmonella Company Name: Natureen International Inc. Brand Name: Brand Name(s) Product Description: Product Description Dried Black Fungus Slice Company Announcement Natureen International Inc. of Walnut, CA is recalling 244…
Infant Breathing System Recall: AirLife/Vyaire Removes Infant Heated Wire Circuits Due to Risk for Inadvertent Adapter Disconnection During Ventilation
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Image A: Adaptors provided in the accessory bag of the AirLife Infant Heated Wire Circuit….
Mondelēz Global LLC Conducts U.S. Voluntary Recall of Four Carton Sizes of RITZ Peanut Butter Cracker Sandwiches Due to Labeling Error
Summary Company Announcement Date: July 08, 2025 FDA Publish Date: July 08, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Allergen – Peanut Company Name: Mondelez Global LLC Brand Name: Brand Name(s) Product Description: Product Description Peanut butter cracker sandwiches Company Announcement EAST HANOVER, N.J., July 8, 2025 –…
Extended-Release Stimulants for ADHD: FDA Drug Safety Communication – FDA Requires Expanded Labeling about Weight Loss Risk in Patients Younger than 6 Years
AUDIENCE: Patient, Health Care Professional, Pharmacy, Pediatrics ISSUE: The FDA is revising the labeling of all extended-release stimulants indicated to treat attention-deficit/hyperactivity disorder (ADHD) – including certain formulations of amphetamine and methylphenidate – to warn about the risk of weight loss and other adverse reactions (side effects) in patients younger than 6 years taking these…
Early Alert: Blood Pump Controller Issue from Abiomed
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. The FDA has become aware of a potentially high-risk issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product The FDA is aware that Abiomed has issued a letter…
Early Alert: Infusion Pump Software Issue from Baxter
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. The FDA has become aware of a potentially high-risk issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product Spectrum V6 infusion pump startup screen Spectrum V8 infusion pump…
Mellace Family Brands California, Inc. Issues An Allergy Alert On Undeclared Milk Allergen In Wegmans Semi-Sweet Chocolate Nonpareils
Summary Company Announcement Date: June 25, 2025 FDA Publish Date: June 30, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk allergen Company Name: Mellace Family Brands California, Inc. Brand Name: Brand Name(s) Product Description: Product Description Semi-sweet Chocolate Company Announcement Mellace Family Brands California, Inc. of Warren, OH…
Resuscitation System Recall: ZOLL Circulation, Inc. Recalls AutoPulse NXT Resuscitation System Due to a Failure Code That May Stop Compressions or Deliver Inadequate CPR
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Product Name: AutoPulse NXT Platform Model: Model 200 Catalog Number: 8700-001070-1 Software Version:…