Summary Company Announcement Date: February 11, 2026 FDA Publish Date: February 12, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Listeria monocytogenes Company Name: Slade Gorton & Co., Inc. Brand Name: Brand Name(s) Wellsley Farms Product Description: Product Description Company Announcement Waltham, Mass. – Slade Gorton & Co., Inc, is recalling…
Emergency Response Safety Kit Recall: Airlife Removes Certain Broselow Pediatric Emergency Rainbow Tapes and Broselow ALS Organizers
The affected products and recommendations for what to do with the devices below have not changed. 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…
Trividia Health, Inc. Initiates Labeling Correction for all TRUE METRIX® Blood Glucose Monitoring Systems
Summary Company Announcement Date: February 06, 2026 FDA Publish Date: February 06, 2026 Product Type: Medical Devices Reason for Announcement: Recall Reason Description As currently written, the Owner’s Booklets/System Instructions for Use fails to emphasize that users must seek medical attention immediately if they receive an E-5 error code and are experiencing symptoms of high…
Glucose Monitor Sensor Recall: Abbott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors
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. The affected products have not changed, but the “Full list of affected lots” has been modified for…
Prime Food Processing LLC Issues Allergy Alert and Safety Warning Regarding Uneviscerated Dried Croaker Fish
Summary Company Announcement Date: February 03, 2026 FDA Publish Date: February 05, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Product was not adequately eviscerated and may harbor harmful bacteria or toxins Company Name: Prime Food Processing LLC Brand Name: Brand Name(s) Product Description: Product Description Dried Croaker Fish…
Detachable Coil System Recall: J&J MedTech/CERENOVUS Inc. Remove CEREPAK Detachable Coil System
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 The FDA is aware that J&J MedTech and their subsidiary, CERENOVUS Inc., have issued a…
Mondelēz Global LLC Expands Voluntary Recall of 2 SKUs of CHIPS AHOY! Baked Bites Brookie in the USA Previous Release Was Issued on December 24, 2025
Summary Company Announcement Date: December 30, 2025 FDA Publish Date: February 04, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Product Safety – choking threats Company Name: Mondelez Global Brand Name: Brand Name(s) CHIPS AHOY Product Description: Product Description Baked brownie bites Company Announcement “This is a recall expansion of a…
Glucose Monitor Sensor Recall: Abott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors
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. The affected products have not changed, but the “Full list of affected lots” has been modified for…
Akkarco LLC Recalls Product Due to Possible Health Risk
Summary Company Announcement Date: January 28, 2026 FDA Publish Date: February 03, 2026 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Product contains tadalafil Company Name: Akkarco LLC Brand Name: Brand Name(s) Ashfiat Alharamain Product Description: Product Description Honey Product for Energy Support Company Announcement Akkarco LLC of Lorton, Virginia, is voluntarily…
Early Alert: Heart Pump Issue from Abiomed
CDRH is issuing this Early Alert to notify the public of a potentially high-risk device 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 an Urgent Medical Device Correction to notify affected customers of updated…