262 recalls tagged with “lithium battery”.
CCCEI Brand power strips are recalled after a potential fire risk due to missing overcurrent protection. The recall covers 6ft, 10ft, and 15ft models sold by Middle Way Electronics. Consumers should stop using the product and request a full refund.
FUNTOK 24V 2-Seater Ride-On Trucks recalled by Shenzhen Luobe Trading Co. for fire and burn hazards. The recall covers model DLS-K03 sold in red, black, white and pink. The company urges consumers to stop using the product and contact for a full refund.
Sunnyyes LED mini lights are recalled after reports of serious injury risk from accessible coin batteries. The recall covers Sunnyyes branded lights sold nationwide. The hazard stems from lithium coin batteries accessible to children, plus a loose remote-control battery screw and missing parental warnings. Stop using the product and contact Sunnyyes for a full refund.
Geri-Care eye drops recalled nationwide after lack of sterility assurance affects 720 bottles. The product, ARTIFICIAL TEARS with NDC 68788-7266-0, is manufactured by Preferred Pharmaceuticals, Inc. in Brooklyn, NY. The FDA recall class II points to a risk of contamination. Stop using immediately and contact a healthcare provider for guidance.
GE Healthcare recalled Omnipaque iohexol injection, 300 mg/mL, distributed nationwide in the United States. The Class II recall covers 866,570 vials due to particulate matter. Healthcare providers should stop use and contact GE Healthcare Ireland Limited for guidance.
GE Healthcare recalled Omnipaque iohexol injection after discovery of particulate matter. The recall covers 306,810 vials distributed nationwide in the United States. WHS: Distributed by GE Healthcare Inc., Marlborough, MA. Consumers should stop use and consult a healthcare provider for guidance.
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
Lifetime Brands recalls BUILT LUUM Light Up Tumblers sold at multiple retailers. The recall covers 16 oz and 18 oz plastic cups with a lid and straw that contain a bottom LED light powered by a button cell battery. Labels on the underside or hangtags show the theme and item numbers with UPCs. Stop using these tumblers immediately and seek a full refund by contacting Lifetime Brands.
Teva Pharmaceuticals USA recalled 19,869 cartons of Octreotide Acetate for Injectable Suspension nationwide in the United States after FDA inspection flagged lack of assurance of sterility at the contract manufacturer. The FDA cited quality system deficiencies at Pharmathen International S.A. in Greece. Healthcare providers and patients should stop using the product immediately and contact Teva or
Teva Pharmaceuticals recalled 1,897 cartons of Octreotide Acetate for Injectable Suspension distributed nationwide in the USA after an FDA inspection flagged sterility concerns. The recall is due to lack of assurance of sterility from the contract manufacturer. Consumers and healthcare providers should stop using the product immediately and contact Teva for guidance.
Honda recalls 2023-2025 Pilot and 2023-2024 Passport vehicles due to potential fuel filler neck tube and pipe separation. The defect can allow fuel leaks with a fire risk. Owners should contact Honda for inspection and repair at no cost. Recall OKM is in effect; letters mailed January 7, 2025.
BD Becton, Dickinson and Company and Fresenius Kabi USA recall 0.9% Sodium Chloride Injection, USP, 250 mL in a single-dose bag nationwide, including Alaska and Puerto Rico. The recall cites lack of assurance of sterility. Healthcare providers and patients should stop using the product immediately and follow guidance from Fresenius Kabi or their provider.
Fresenius Kabi USA, LLC recalls 5% Dextrose Injection, USP 12.5 g per 250 mL in FreeFlex bags due to lack of sterility assurance. The recall covers units distributed nationwide including Alaska and Puerto Rico. Healthcare providers and patients should stop use and consult a healthcare professional.
Siemens Medical Solutions USA recalled 758 units in the U.S. and 2,077 outside the U.S. of ARTIS pheno and ARTIS Icono imaging systems after a dose-display anomaly could misrepresent high X-ray doses. The devices may still be within regulatory dose limits, but the displayed dose may appear significantly higher. Clinicians should stop using the devices and await manufacturer guidance.
Cook Incorporated recalls 104 Wayne Pneumothorax Sets worldwide after labeling errors show expiration dates exceeding true shelf life. The recall affects reference parts C-UTPT-1020-WAYNE-IMH and C-UTPT-1400-WAYNE-112497-IMH with order numbers G56532 and G56535. Healthcare providers should stop use immediately and follow recall instructions.
Cook Medical recalled 49 units of the Strange Bile Duct Stone Exploration Set due to labels showing expiration dates beyond shelf life. The recall is worldwide and active as of March 5, 2026. Healthcare providers were advised to stop use and follow recall instructions.
Toyota recalls 2022-2025 Tundra and Tundra Hybrid vehicles because moisture in the reverse light assemblies can cause light failure. Dealers will replace both reverse light assemblies and repair wire harnesses. Owner letters were mailed September 11, 2025. Contact Toyota at 1-800-331-4331 for recall 24TB06 and 24TA06.
Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips instructions.
Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.
Philips is recalling 798 Azurion 3 M15 systems worldwide, including 42 units in the United States. The wired foot switch may fail to initiate X-ray imaging or fail to produce consistent imaging. Healthcare providers should stop using the affected devices and follow recall instructions issued by Philips.