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.
1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
KingPavonini recalled six models of adult portable bed rails due to serious risks of entrapment and asphyxiation. The recall affects products sold on Amazon since November 2025. Consumers must stop using these bed rails immediately and seek a refund or replacement.
Winder Laboratories, LLC recalled 3,528 bottles of Morphine Sulfate Oral Solution on November 26, 2025. The labeling error misrepresented the product size, leading to potential dosing issues. Consumers should stop using the product immediately and consult their healthcare provider.
Macardac recalled baby loungers on November 26, 2025, due to serious risks of entrapment and falls. The loungers violate safety standards for infant products. Consumers should stop using the loungers immediately and seek a refund.
Alinux recalled its baby loungers on November 26, 2025, due to serious injury or death risks from entrapment and fall hazards. The loungers do not comply with mandatory safety standards for infant sleep products. Consumers should stop using them immediately and seek a refund.
Walmart recalled Ozark Trail Tabletop 1-Burner Butane Camping Stoves on November 26, 2025. The stoves pose serious burn and fire hazards due to possible explosions. Consumers should stop using the product immediately and return it for a full refund.
Bosen US recalled Sofoliana and Glotika baby loungers on November 26, 2025. The loungers pose risks of serious injury or death due to entrapment and fall hazards. The product violates mandatory safety standards for infant sleep products.
Vivohome recalled adult portable bed rails on November 26, 2025, due to serious injury hazards. The recalled rails can pose risks of entrapment and asphyxiation. Consumers should stop using them immediately and seek a refund.
McLee Creations recalled MyOnlyStyler Root Booster Hair Dryers on November 26, 2025, due to electrocution hazards. The recalled model, MOS-22, was sold in white with black bristles. Consumers should stop using the product immediately and return it for a refund.
Outdoor Master recalled two models of children's and youth helmets on November 26, 2025. The helmets violate mandatory safety standards and pose a risk of serious head injury. Consumers should stop using them immediately and seek refunds.
Cook Medical recalled 15 units of Transjugular Intrahepatic Access Sets on November 26, 2025. The devices may have been manufactured out of specification, leading to potential complications during medical procedures. Patients and healthcare providers should stop using these devices immediately.
Cook Medical recalled 7,952 Flexor Check-Flo introducers and sets on November 26, 2025. The devices may have been manufactured out of specification, potentially posing serious risks to patients. Health care providers and patients should stop using these products immediately.
Cook Medical recalled 23 units of its Transjugular Liver Access Sets on November 26, 2025. The recall follows concerns that products may have been manufactured out of specification, leading to potential use errors. Healthcare providers and patients should stop using the device 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.
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.