These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Medline Industries recalled 15,581 electric homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat, posing a risk of fire in rare cases. The recall follows 58 complaints of sparking or burning from the pendant.
Medline Industries recalled 13,245 homecare beds on November 26, 2025, due to a fire risk from the hand control pendant. The company received 58 reports of sparking, burning, and smoke. Patients and healthcare providers must stop using the beds immediately and follow recall instructions.
Ferndale Laboratories recalled 24,589 vials of Mastisol Liquid Adhesive due to a defect. The butyrate tube may crack during use, making the product unusable. The recall affects products distributed in the U.S. and the U.K., announced on November 25, 2025.
Prairie Farms Dairy recalled 3,752 gallons of Fat Free Milk on November 25, 2025. The milk may contain food-grade cleaning agents, posing a health risk. Consumers should not consume the product and seek refunds or replacements.
Imu-Tek Animal Health recalled 113 bottles of Immuno-5 Colostrum Powder on November 25, 2025. The product contains an undeclared milk allergen, posing a risk to consumers with milk allergies. The recall affects states including CA, TX, and FL.
Abbott Diabetes Care recalled over 1 million FreeStyle Libre 3 sensors on November 24, 2025, due to a manufacturing issue. The defect may lead to incorrect low glucose readings, posing a serious health risk. Affected sensors were distributed across the U.S. and several international markets.
Alcon Laboratories, Inc. recalled 151 units of Custom Pak surgical procedure packs on November 24, 2025. The recall stems from incomplete seals that may affect sterility. Healthcare providers and patients should stop using the products immediately.
Breckenridge Pharmaceutical, Inc. recalled 7,389 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations and the presence of N-nitroso-duloxetine impurity above FDA limits. Consumers should stop using the product immediately and contact healthcare providers for guidance.
Towa Pharmaceuticals recalled 3,397 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations resulting in N-nitroso-duloxetine levels exceeding FDA limits. Consumers must stop using the product immediately.
Gimme Coffee, Inc. recalled 252 boxes of Decaf de Agua coffee pods on November 24, 2025. The product contains undeclared caffeine, posing a risk to consumers sensitive to caffeine. Affected products include those with best-by dates of September 30, 2025, and October 15, 2025.
Bell Industries recalled 66 units of Zen Cleanse Blend herbal tea on November 24, 2025. The recall follows potential Salmonella contamination. The product was distributed to three customers in Massachusetts, Texas, and Wisconsin, but did not reach retail shelves.
Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.
Draeger, Inc. recalled 431 units of the Vapor 2000 anesthetic vaporizer on November 24, 2025. A component of the devices contained impurities and did not meet specifications, posing a high hazard risk. Healthcare providers and patients should cease use immediately and follow recall instructions.
ICU Medical recalled the LifeShield Infusion Safety Software Suite v2.2 on November 24, 2025. The software fails to operate as expected for migrated libraries, risking medication delivery errors. The recall affects seven customers across several states, including California and New York.
ICU Medical recalled LifeShield Drug Library Management software on November 24, 2025. A software issue limits concentration precision to one decimal place, risking incorrect drug dosages. Users should stop using the product immediately and follow recall instructions.
Abbott Diabetes Care recalled 258,913 FreeStyle Libre 3 Plus sensors on November 24, 2025. Manufacturing issues may lead to incorrect low glucose results, posing a high risk to users. Consumers should stop using the device immediately and follow the recall instructions.
Abbott Diabetes Care recalled 1,663,241 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may lead to incorrect low glucose results, creating serious health risks for users. Patients should stop using the sensors immediately and follow recall instructions.
Abbott Diabetes Care recalled 8,062 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may cause inaccurate low glucose readings, posing serious health risks. Consumers should stop using the device immediately and follow recall instructions.
Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.
GBC Food Services recalled EverRoast Chicken Caesar Salad on November 22, 2025, due to potential Listeria monocytogenes contamination. The recall affects 2 units of the product distributed in Kentucky and Indiana. Consumers should not consume this product and seek a refund or replacement.