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.
2,168 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Bazic Products recalled Bazic Silicone Glue on January 29, 2026, due to a serious poisoning risk for children. The glue's packaging does not meet child-resistant standards, violating federal law. Consumers should stop using the product immediately and seek a full refund.
LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.
Mindbodygreen recalled Ultimate Multivitamin+ dietary supplements on January 29, 2026, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating safety standards. Consumers should stop using the product immediately and secure it out of children's reach.
Northern Tool + Equipment recalled three models of hot water pressure washers on January 29, 2026. Abnormal burner operation can produce smoke and flames, posing a fire hazard. Consumers should stop using the products immediately and seek repairs.
Nengmiaokeji recalled Sefudun 5% Minoxidil Hair Growth Serum Kit on January 29, 2026. The product lacks child-resistant packaging, posing a serious poisoning risk to children. Consumers should stop using the serum immediately and contact the company for a replacement.
Viofairy recalled its Hair Growth Serum on January 29, 2026, due to serious poisoning risks. The packaging lacks required child-resistant features, endangering young children. Consumers must stop using the product immediately and secure it out of reach.
Preema brand recalled 720 bottles of Bright Red and Orange Food Colour Powders on January 29, 2026. The products contain a banned color, carmoisine, and undeclared FD&C Yellow 5 and FD&C Red 40. Consumers should not consume these products and seek refunds immediately.
Khee Trading Inc. recalled 7,306 cases of Frozen Half Shell Oysters on January 27, 2026. The oysters may be contaminated with Norovirus, posing a serious health risk. Consumers should not consume the product and seek a refund or replacement.
Beacon Promotions recalled 5,788 units of repackaged M&Ms candies on January 26, 2026. The candies contain undeclared allergens, specifically milk, soy, and peanuts. Consumers should not consume these products and should seek refunds.
Asteria Health recalled 24,099 Estradiol, 10 mg pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately. The recall affects pellets distributed nationwide in the USA.
Beacon Promotions recalled 541 units of repackaged M&Ms Peanut candies on January 26, 2026. The candies contain undeclared allergens including milk, soy, and peanuts. Consumers should stop using the product immediately and seek a refund or replacement.
Asteria Health recalled 1,464 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects products distributed nationwide. Consumers must stop using the product immediately and seek guidance from healthcare providers.
Granules Pharmaceuticals Inc. recalled 71,424 bottles of Trazodone Hydrochloride on January 26, 2026. The recall stems from the presence of foreign tablets or capsules in the product. Consumers should stop using the medication immediately and consult their healthcare provider.
Philips Medical Systems recalled 326 Azurion 5 M12 systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a risk to patients and healthcare providers. Immediate cessation of use is advised.
Philips Medical Systems recalled 1,503 Azurion 7 B20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a risk of injury. Healthcare providers must stop using the device and follow recall instructions immediately.
Philips Medical Systems Nederland B.V. recalled 922 Azurion 5 M20 systems on January 26, 2026, due to a defect that causes unexpected table movement. This hazard can occur even with an active table lock when the Reset Geometry button is pressed. The recall includes 101 units in the U.S. and 821 units distributed worldwide.
Philips Medical Systems recalled 291 Azurion 3 M12 systems on January 26, 2026, due to a risk of unexpected table movement. This may occur when the Reset Geometry button is pressed, even if a table lock is active. The recall affects 27 units in the U.S. and 264 units internationally.
Philips Medical Systems Netherlands B.V. recalled 655 Azurion 7 B12 systems on January 26, 2026. The recall affects models 722067, 722225, and 722235 due to unexpected table movement when the Reset Geometry button is pressed. This poses a high risk of injury to patients and healthcare providers.
Philips Medical Systems recalled 1,979 Azurion 7 M12 Systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a high risk of injury. Healthcare providers and patients should stop using the devices immediately.
Asteria Health recalled 50,990 Estradiol pellets on January 26, 2026, due to potential metal particulate matter contamination. The recall affects products distributed nationwide in the USA. Consumers should stop using the pellets immediately and seek guidance from healthcare providers.