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.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Asteria Health recalled 1,758 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects pellets distributed nationwide in the USA. Consumers should stop using the product immediately and contact their healthcare providers for guidance.
Asteria Health recalled 3,871 testosterone pellets on January 26, 2026, due to potential metal particulate matter. The recall affects products distributed nationwide in the USA. Consumers should stop using the product immediately and seek guidance from their healthcare providers.
Asteria Health recalled 100 sterile pellets of testosterone and anastrozole on January 26, 2026. The recall stems from potential metal particulate contamination. Consumers must stop using the product immediately and consult healthcare providers for guidance.
Asteria Health recalled 22,478 Estradiol 12.5 mg pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The FDA classified this recall as Class II, indicating a high hazard level.
Asteria Health recalled 70,959 testosterone pellets on January 26, 2026, due to potential metal contamination. Consumers must stop using the product immediately. The recall affects multiple lots distributed nationwide in the USA.
Asteria Health recalled 670 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The recall affects all units distributed nationwide in the United States.
Philips Medical Systems recalled 5,136 Azurion 7 M20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a danger to patients and healthcare providers. Consumers should stop using the devices immediately and contact the manufacturer for instructions.
Philips Medical Systems Nederland B.V. recalled 802 Azurion 3 M15 systems on January 26, 2026. The systems may move unexpectedly, posing a risk to patients and healthcare providers. Consumers should stop using the device immediately and follow recall instructions.
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.
Aborder Products recalled Cumbor retractable safety gates on January 22, 2026, due to a serious entrapment risk for children. The gates can allow a child's torso to fit through the opening, posing a high risk of injury or death. Consumers must stop using the gates immediately and contact the company for a full 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.
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.
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.
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.
Red Button Movie House recalled 6,480 packages of popcorn on January 22, 2026, due to possible foreign material contamination. The affected popcorn packs weigh 24 ounces and were distributed across several states including Utah and Colorado. Consumers should not consume this product and seek refunds immediately.
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 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.