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 Medline has issued a letter to affected customers recommending…
Abbott Initiates Medical Device Correction for Certain FreeStyle Libre® 3 and FreeStyle Libre 3 Plus Sensors in the U.S.
Summary Company Announcement Date: November 24, 2025 FDA Publish Date: January 15, 2026 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Internal testing determined that some sensors may provide incorrect low glucose readings. Company Name: Abbott Brand Name: Brand Name(s) FreeStyle Libre Product Description: Product Description FreeStyle Libre 3 and 3 Plus Glucose…
Spring & Mulberry Expands Voluntary Recall of Select Chocolate Bars Due to Possible Salmonella Contamination
Summary Company Announcement Date: January 14, 2026 FDA Publish Date: January 15, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Spring & Mulberry Brand Name: Brand Name(s) Spring & Mulberry Product Description: Product Description Multiple Flavors of Chocolate Bars Company Announcement Raleigh,…
Superfoods Inc. dba Live it Up. Recalls Live it Up Super Greens Because of Possible Health Risk
Summary Company Announcement Date: January 15, 2026 FDA Publish Date: January 15, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Superfoods, Inc. DBA as Live it Up Brand Name: Brand Name(s) Live it Up Product Description: Product Description Super Greens Original and…
Early Alert: Dialysis Tubing Set Issue from Vantive
The FDA has become aware 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 Vantive has issued a letter informing affected customers that Prismaflex Control Units have updated use instructions. Affected devices: Device…
Diva Fam Inc. Announces Voluntary Recall Of Sea Moss Gel Superfood Products Due to Possible Health Risk
Summary Company Announcement Date: January 09, 2026 FDA Publish Date: January 12, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Botulism Company Name: Diva Fam Inc. Brand Name: Brand Name(s) True Sea Moss Product Description: Product Description Sea Moss Gel Superfood in various flavors (16…
Food Business Karison Foods & Snacks Inc Recalls ‘PANJIRI’, ‘ALSI PINNI’, ‘PUNJABI PINNI’, ‘BESAN LADDOO’, and ‘NO SUGAR ADDED BESAN LADDOO’ Due to Undeclared Milk Allergen
Summary Company Announcement Date: January 12, 2026 FDA Publish Date: January 12, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Milk Company Name: Karison Foods & Snacks Inc Brand Name: Brand Name(s) Product Description: Product Description Panjiri, pinni, and laddoo Company Announcement Karison Foods &…
Spring & Mulberry Issues Voluntary Recall of Mint Leaf Date Sweetened Chocolate Bar Due to Possible Salmonella Contamination
Summary Company Announcement Date: January 12, 2026 FDA Publish Date: January 12, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Spring & Mulberry Brand Name: Brand Name(s) Spring & Mulberry Product Description: Product Description Mint Leaf Date Sweetened Chocolate Bar Company Announcement…
Infusion Pump Recall: Fresenius Kabi Removes Ivenix Large Volume Pumps
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 Fresenius Kabi has issued a letter to affected customers recommending…
VH Foods Inc. DBA Outside The Breadbox Issues Allergy Alert on Undeclared Egg and Milk in “Bread Crumbs”
Summary Company Announcement Date: January 12, 2026 FDA Publish Date: January 12, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Egg and Milk Company Name: VH Foods Inc. DBA Outside The Breadbox Brand Name: Brand Name(s) Outside the Breadbox Product Description: Product Description Bread Crumbs…