Browse through 474 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Aiho recalled five-drawer dressers on July 24, 2025, due to tip-over and entrapment hazards. The dressers, model number AP23-W, do not meet safety standards set by the STURDY Act. Consumers should stop using the product if it is not anchored to a wall.
Apollo recalled certain electric scooters on July 24, 2025, due to a welding defect. The defect can cause the stem to break, leading to falls and injuries. Consumers should stop using the scooters and contact Apollo for a free replacement.
LIVACTI recalled retractable safety gates on July 24, 2025, due to serious entrapment hazards. The gates can pose a risk of injury or death to children. Consumers should stop using them immediately and seek refunds.
FENGQS recalled F7 Pro electric bikes on July 24, 2025, due to fire hazards. The lithium-ion batteries can overheat and ignite, posing serious risks. Consumers should stop using the bikes immediately and seek refunds.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.
Middlefield Original Cheese Co-op recalled 246.5 pounds of 100% Grass-Fed Pepper Jack Cheese on July 21, 2025. The cheese may be contaminated with Listeria monocytogenes, which can cause serious illness. Consumers should not eat this product and seek a refund.
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese on July 21, 2025. The recall affects Monterey Jack and Farmers Cheese due to potential Listeria monocytogenes contamination. The products were distributed in Kentucky, Ohio, and Pennsylvania.
AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.
Bestway, Intex, and Polygroup recalled certain above-ground pools due to a drowning hazard. Nine deaths have been reported linked to this issue. The recall affects about five million pools sold since 2002.
Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets on July 21, 2025. The recall stems from a failure in dissolution specifications that could delay drug release. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Ascend Laboratories recalled 8,568 bottles of Amlodipine and Olmesartan Medoxomil Tablets on July 21, 2025. The recall follows reports of low dissolution results, impacting the drug's effectiveness. Consumers should stop using the product and seek guidance immediately.
DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.
DJO Surgical recalled 927 units of the Altivate Reverse Wedge Glenoid Reamer Head on July 18, 2025. The recall follows reports that the device may kick or bind up during use. Healthcare providers and patients must stop using the product immediately.
DJO Surgical recalled 907 units of the Altivate Reverse Wedge Glenoid Reamer on July 18, 2025, due to a kickback risk during use. The recall affects healthcare providers and patients nationwide across 25 states. This Class II recall warns of potential binding issues that could lead to serious injury.
DJO Surgical recalled 439 AltiVate Reverse Glenoid Trays on July 18, 2025, due to potential reamer malfunction. The reamer may kick or bind during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow the recall instructions.
Tractor Supply recalled multiple models of its Traveller aluminum loading ramps on July 17, 2025. These ramps can bend or break under weight, posing a fall hazard. Consumers should stop using them immediately and seek refunds.
Primark recalled DTR Stitch Scented Highlighters on July 17, 2025, due to phthalate exposure. The highlighters, resembling slushie containers, pose a health risk to children. Consumers should stop using them immediately and seek a refund.
VIVI recalled lithium-ion batteries for e-bikes on July 17, 2025. The batteries can overheat, posing fire and burn hazards. Consumers must stop using the affected e-bikes immediately.
C.R. Bard recalled 4,300 Foley catheter trays on July 17, 2025. Incorrect inserts may lead users to misidentify materials, increasing infection and allergic reaction risks. Patients and healthcare providers must stop using the trays immediately and follow recall instructions.
Babyletto recalled its Kiwi Electronic Recliner on July 17, 2025, due to a fire hazard. The USB module can overheat and spark, posing a risk to users. Consumers should stop using the recliners immediately and contact Babyletto for a repair kit.