370 recalls tagged with “nhtsa regulated”.
B Braun Medical recalls 12,168 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The backflow of medication from secondary to primary containers and the inability to prime pose a high-risk issue. Stop using the device immediately and follow manufacturer instructions.
Water Pure is recalling 17,612 bottles of My Bladder dietary supplement sold nationwide after an FDA notice cited possible contamination with E. coli O7:K1 and E. coli 1303. The contamination could cause illness. Consumers should not consume the product and should contact Water Pure for refund or replacement information.
3M and its Scotch brand recalled the TL909-50 thermal laminator sold at Office Depot, Office Smart and School Specialty from August 2024 through September 2025. The units may overheat, creating a burn hazard. Consumers should stop using the recalled laminator, unplug it and contact 3M for a full refund.
Olympia Tools International recalls Pack-N-Stroll Premium Folding Utility Wagons sold at Costco after authorities determined the product can trap a child’s head and cause serious injury or death. The defect is an opening between the organizational tray and the sidewall. The wagon also lacks a restraint system. Stop using the wagon now and return it to Costco for a full refund.
No injuries have been reported. Cranach Hardware recalled tip restraint kits sold through retailers after testing showed the plastic brackets and tie can fail to meet safety standards. Stop using the restraints and contact Cranach Hardware for a free stainless steel replacement kit.
Sauna360 recalls Tylö Halmstad and Kiruna Hybrid saunas sold by Sauna360 distributors nationwide from July 2024 through December 2024 for between $6,000 and $12,000. The recall targets bench seating that can collapse, creating a fall hazard. Stop using the benches immediately and contact Sauna360 for a free repair.
M.C.I. Foods recalled 330 cases of Cheese and Egg with Green Salsa Breakfast Burrito sold to seven distributors nationwide. The ready-to-eat burrito contains a cooked egg ingredient that tested positive for Listeria monocytogenes. Consumers should not eat the product and should contact M.C.I. Foods for refund or replacement by letter.
Paragon 28 recalled 20 Phantom Fibula Nails nationwide after finding out-of-spec thread depths. The defect may prevent the nail from mating properly with the mounting bolt. Surgery could be aborted if the implant cannot mate with instrumentation. Hospitals and surgeons should stop using the device immediately and follow recall instructions.
DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.
Major Pharmaceuticals recalled Gabapentin Capsules, USP, 100 mg, 10 capsules per blister pack, distributed nationwide in the United States. The recall cites failed impurities and degradation specifications from routine stability testing, specifically an out-of-spec Highest Unknown Impurity. Consumers and healthcare providers should stop using this product immediately and contact The Harvard Drug集团
CA Botana International recalled 1,167 tubes of Doctor. D. Schwab Mineral Sunscreen SPF 50 after CGMP deviations were found. The recall cover identifies lot D54596 with exp 1/31/2028. The distribution includes California, Colorado, Florida, Puerto Rico and Washington.
Lannett Company, Inc. recalled 46,848 bottles of NIACIN Extended-release Tablets, 1,000 mg, Rx Only, distributed nationwide. The product failed dissolution specifications. Patients and healthcare providers should stop using it immediately and await recall instructions.
A recall is active for Elixir by Coco March Tinted Mineral Sunscreen SPF 50 amid CGMP deviations. The product is distributed by CA Botana International, Inc. The recall cites CGMP deviations as the hazard and class II designation. Consumers should stop using the product and follow guidance from healthcare providers.
STAQ Pharma recalled Ketamine Hydrochloride injections distributed nationwide in the United States. The labeling has incorrect or missing lot and expiration date information. Stop using the product and contact STAQ Pharma or your healthcare provider for guidance.
AstraZeneca recalls 916 Fasenra benralizumab injections distributed nationwide in the United States. The lot is YJ0152 and the NDC is 0310-1730-30. The product is being recalled for lack of sterility assurance. Stop using this product immediately and contact AstraZeneca for guidance.
Rising Pharma Holdings recalled 2,064 bottles of Carbidopa, Levodopa and Entacapone tablets distributed nationwide in the United States. Sealed bottles labeled 25 mg/100 mg/200 mg contained 37.5 mg/150 mg/200 mg instead. Healthcare providers and patients should stop using immediately and await recall letter guidance.
Viona Pharmaceuticals recalled 13,080 Tavaborole Topical Solution 5%, 10 mL bottles distributed nationwide in the United States. The recall covers Tavaborole Topical Solution 5%, Rx only, manufactured by Zydus Lifesciences Ltd. Discoloration linked to RES #97424 prompted the action. Consumers should stop using the product and contact Viona for guidance.
Volkswagen Group of America recalls 2025 ID. Buzz vehicles due to an incorrect brake warning light symbol and color on the instrument panel. Dealers will update the instrument panel software at no charge. Letters notifying owners were mailed June 6, 2025. Contact VW at 1-800-893-5298 for recall 90A2.
Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.
Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 interventional fluoroscopic x-ray systems distributed in 14 countries. The defect is corrosion of the IITV control board that may cause loss of imaging functionality or poor image quality. Healthcare providers and patients should stop using the device and follow manufacturer instructions for recall remediation.