1,716 recalls tagged with “cpsc regulated”.
J2C Hawaii recalled Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel on January 30, 2026. The recall affects approximately 300 units distributed in Hawaii. The product mislabels peanuts, posing a risk to consumers with peanut allergies.
Reser's Fine Foods recalled 298 tubs of Tuna Salad on January 30, 2026 due to undeclared fish allergens. The product was mislabeled with a Chicken Salad lid, posing a risk to consumers with fish allergies. The recall affects distribution in Arizona, California, Nevada, Utah, and Washington.
AiTuiTui recalled its Pull String Teething Toys on January 29, 2026, due to a choking risk. The toys do not meet mandatory safety standards, posing a potential risk of serious injury or death. Consumers should stop using the teething toys immediately and contact the manufacturer for a refund.
Hobby Lobby recalled above-ground pools manufactured by Starmatrix Group on January 29, 2026. The pools pose a drowning risk due to a design flaw that creates a foothold for children. Consumers should stop using these pools immediately and contact Starmatrix for a free repair kit.
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.
Olympus Corporation of the Americas recalls 1,276 boxes of MAJ-1218 Single Use Biopsy Valve distributed nationwide to healthcare facilities. The device risks rubber fragment detachment during use. Stop using the device and follow the recall instructions from Olympus or your healthcare provider.
Teva Pharmaceuticals recalled 67,043 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg, distributed nationwide. The FDA enforcement report cites Failed Dissolution Specifications as the hazard. Health care providers and patients should stop using this product immediately and contact Teva for guidance.
Teva Pharmaceuticals recalled 7,448 bottles of Metoprolol Succinate Extended-Release Tablets nationwide after failed dissolution specifications were identified. The recall involves 100 mg, 100‑tablet bottles (NDC 45963-677-11) and 1,000‑tablet bottles (NDC 45963-677-96). The defect may affect drug release and efficacy. Patients should stop using affected bottles and contact Teva or their clinician
Ultradent Products recalled 2,508 Jiffy Original Composite Polisher Cups (Coarse) 12pk across multiple U.S. states. A defect causes cups to crumble and break apart, potentially delaying patient treatment. Clinicians should stop using the cups immediately and follow the manufacturer’s recall instructions.
Art Monkey LLC recalled 8,500 bottles of Why Not Natural Moringa Capsules on January 28, 2026. The capsules may be contaminated with Salmonella and pose a serious health risk. Consumers should stop using the product immediately and seek refunds.
Koi Koi Trading recalled 3,884 cases of frozen fish balls on January 28, 2026. The recall was issued due to undeclared allergens, Wheat and Sesame, posing a serious health risk. Consumers should stop using the product immediately and seek a refund.
Abiomed recalled 4,496 Impella RP Flex with SmartAssist devices. The recall cites a differential pressure sensor that may malfunction and drift readings. Stop using the device immediately and follow the manufacturer's recall instructions.
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.
Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.
Abiomed recalled 291 Impella RP with SmartAssist devices sold worldwide, including the US. A differential pressure sensor may malfunction and cause readings to drift. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
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.