Summary Company Announcement Date: April 28, 2025 FDA Publish Date: April 29, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Milk Company Name: Taylor Fresh Foods Brand Name: Brand Name(s) Trader Joe’s Product Description: Product Description Sesame Miso Salad with Salmon Company Announcement FOR IMMEDIATE…
Mauna Loa Macadamia Nut Company, LLC Issues Allergy Alert on Undeclared Almonds and Cashews in Mauna Loa Dark Chocolate Covered Macadamias (0.6OZ and 4OZ)
Summary Company Announcement Date: April 26, 2025 FDA Publish Date: April 26, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared cashew, almond Company Name: Mauna Loa Macadamia Nut Company LLC Brand Name: Brand Name(s) Product Description: Product Description Dark Chocolate Covered Macadamias Company Announcement Mauna Loa Macadamia Nut Company LLC…
My Life Inc Issues Allergy Alert on Undeclared Milk in ML Natural Premium Quality Lactoferrin as Apolactoferrin
Summary Company Announcement Date: April 25, 2025 FDA Publish Date: April 25, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared milk Company Name: My Life Inc. Brand Name: Brand Name(s) ML Natural Product Description: Product Description Lactoferrin as Apolactoferrin Company Announcement April 25, 2025, My Life Inc. of Federal…
Risk of False Positive Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication
Date Issued: April 24, 2025 The U.S. Food and Drug Administration (FDA) is alerting health care providers and laboratory staff of reports that falsely elevated (false positive) results have occurred when using ASP Global’s RAM Scientific SAFE-T-FILL Micro Capillary Blood Collection tubes with the LeadCare Testing Systems. These tests may overestimate blood lead levels and…
Heart Pump Accessory Removal: Abbott Removes HeartMate Mobile Power Unit due to Instances of Sudden Power Loss
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 Names: HeartMate Mobile Power Unit (MPU) used with the HeartMate 3 Left Ventricular Assist…
New England Village Foods Issues Allergy Alert on Undeclared Almonds in “19th Hole Snack Mix”
Summary Company Announcement Date: April 24, 2025 FDA Publish Date: April 24, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared almonds Company Name: New England Village Foods Brand Name: Brand Name(s) New England Village Snacks Product Description: Product Description 19th Hole Snack Mix Company Announcement New England Village Foods…
FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
Summary Company Announcement Date: April 18, 2025 FDA Publish Date: April 18, 2025 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Distal Tip Design outside scope of 510k clearance Company Name: Q’Apel Medical, Inc. Brand Name: Brand Name(s) Q’Apel Medical Product Description: Product Description 072 Aspiration System Company Announcement Fremont, CA – April…
Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter
Summary Company Announcement Date: April 18, 2025 FDA Publish Date: April 18, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Product may contain an inert fiber identified as polypropylene fibers from the IV bag Company Name: Amneal Pharmaceuticals LLC. Brand Name: Brand Name(s) Amneal Pharmaceuticals LLC. Product Description: Product Description Ropivacaine Hydrochloride Injection,…
Early Alert: Diagnostic Intravascular Catheter Issue from Conavi
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 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 Conavi has issued a…
Recall Reminder: Gerber Products Company Previously Recalled and Discontinued All Batches of Gerber® Soothe N Chew® Teething Sticks Due To Potential Choking Hazard
Summary Company Announcement Date: April 18, 2025 FDA Publish Date: April 18, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential choking hazard for babies and young children Company Name: Gerber Products Company Brand Name: Brand Name(s) Product Description: Product Description Gerber® Soothe N Chew® Teething Sticks Company Announcement ARLINGTON, Va.,…