Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Academy Sports + Outdoors recalled Magellan-branded Odyssey Rocker Chairs on January 22, 2026. The recall affects chairs with date codes 07/2025 and 08/2025 sold from September to October 2025. The chairs have a risk of leg breakage, posing fall hazards to users.
Based Online recalled Fidget Magnet Ball Toy Sets on January 22, 2026, due to a serious ingestion hazard. The toys contain loose high-powered magnets that pose risks of severe injury or death if swallowed. Consumers should stop using these toys immediately and seek a refund.
Iristar recalled Minoxidil Spray Bottles on January 22, 2026, due to a serious poisoning risk to children. The product fails to meet child-resistant packaging standards mandated by the Poison Prevention Packaging Act. Consumers should stop using the product immediately and secure it out of children's reach.
Johnson Health Tech expanded its recall of Matrix and Vision treadmills due to fire hazards. The affected models include T30, TF30, T50, TF50, T75, and others. Consumers should stop using these treadmills immediately and check for a power cord bracket.
Mikario Trading recalled 5,000 convertible baby gyms on January 22, 2026, due to a suffocation risk. The baby gyms violate safety standards for infant support cushions. Consumers must stop using the product immediately and seek a refund.
Yetonamr recalled Pull String Teething Toys on January 22, 2026, due to choking risks. The toys violate safety standards with silicone strings that can obstruct breathing. Consumers must stop using the toys immediately and seek refunds.
Topkay recalled torch lighters on January 22, 2026, due to serious fire and burn hazards. The lighters lack required child-resistant features, posing risks to consumers. The recall affects lighters sold on Amazon by Xiyude.
Vndueey recalled its Magnetic Men toy sets on January 22, 2026, due to ingestion hazards. The sets contain loose magnets that can pose serious health risks to children. Consumers should immediately stop using the toys and seek a refund.
Gagaku recalled ice cream shop toy playsets on January 22, 2026, due to a magnet ingestion hazard. The toys can pose serious injury or death risks if magnets detach and are swallowed. Consumers should stop using the toys and seek a refund immediately.
Thrasio recalled Angry Orange Enzyme Stain Removers on January 22, 2026. The products may contain the bacteria Pseudomonas aeruginosa, posing serious health risks. Consumers should stop using the product and seek a refund immediately.
Unichem Pharmaceuticals recalled Bisoprolol Fumarate and Hydrochlorothiazide tablets on January 21, 2026. The recall affects tablets that do not meet impurity specifications for N-Nitroso Bisoprolol. Consumers should stop using the product and contact their healthcare provider immediately.
Physio-Control recalled 16,499 Infant/Child Reduced Energy Defibrillator Electrodes after reports of delamination. This defect can significantly reduce the effectiveness of the defibrillation. Healthcare providers and patients must stop using the electrodes immediately and follow the recall instructions.
Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.
STAAR Surgical AG recalled 7 EVO+ Visian TICL VTICM5 lenses after finding a labeling error that listed 12.1 mm length but which are 12.6 mm. The mismatch can cause excessive vault and ocular complications. Physicians and patients should stop using the device immediately and follow manufacturer instructions for recall actions.
Auris Health recalled 173 bronchoscopy devices due to a software malfunction. This issue could lead to improper robotic arm positioning, risking patient safety. The recall affects devices distributed nationwide and in Canada, with the announcement made on January 21, 2026.
Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.
Agiliti Health recalled 4,286 Adapt Pumps on January 21, 2026, after identifying a malfunction. The issue prevents the Microclimate Management function from re-engaging following the Autofirm function. This defect poses a risk to patients relying on the device for safe pressure management.
Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.
Dynarex recalled 1,000-pack BZK Antiseptic Towelettes nationwide after CGMP Deviations were identified. The product contains benzalkonium chloride 0.13% and carries NDC 67777-245-04. Consumers should stop using this product immediately and await recall notification by letter.
ACME United recalled WP WipesPlus Hand Sanitizing Wipes, 100-count, sold nationwide, after CGMP deviations were identified. The recall is classified as Class II. Consumers should stop using the product immediately and await guidance from ACME United. The NDC is 67151-727-01.