262 recalls tagged with “lithium battery”.
Belkin is recalling its MMA008 charging stand and BPB002 and PB0003 power banks sold at multiple retailers due to a fire and burn hazard. The lithium-ion battery can overheat. Consumers should stop using the recalled devices immediately and contact Belkin for a full refund or store credit.
Great Lakes Wholesale International recalled Great Lakes Select Battery Packs sold by multiple wholesalers nationwide. The packaging lacks child-resistant features for button cell and coin batteries. Stop using the packs now and contact the company for a full refund.
Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.
STIHL is recalling BR 800 Magnum backpack blowers sold through authorized STIHL dealers from May 2025 through September 2025. The recall targets units with serial numbers 546515117 to 547916107. The fan wheel inside the blower can break apart, creating a laceration hazard. Consumers should stop using the recalled units and bring them to an authorized STIHL servicing dealer for a free inspection is
Peloton recalled Original Series Bike+ units with model PL02 and serials beginning with the letter 'T'. The seat post assembly can break during use, creating a fall and injury risk. Consumers should stop using the recalled bikes and contact Peloton for a free repair.
Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.
GET TESTED INTERNATIONAL AB recalled 19 Hair Mineral Analysis devices distributed nationwide in the United States. The recall cites distribution without premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and contact GET TESTED INTERNATIONAL AB or their healthcare provider for instructions.
Get Tested International AB recalled 1,210 units of its 3 in 1 STI Test distributed nationwide in the U.S. The product was distributed without FDA premarket approval or clearance. Patients and healthcare providers should stop using the device immediately and follow the recall instructions.,
Knog is recalling Blinder 900 and Blinder 1300 Front Bicycle Lights sold at multiple retailers. The recall covers units with batch codes printed on the underside. The lithium-ion battery can overheat and ignite, creating a fire and burn risk. Stop using the recalled lights and register for a free replacement at knog.com/recall.
B. Braun Medical Inc. recalls 300 extension sets used with Infusomat Space and other pumps. The recall flags potential backflow from piggyback IV containers into primary IV containers and the inability to prime. Hospitals should stop using the device immediately and follow recall instructions.
BBMI recalled 63,192 IV administration sets worldwide on Oct 29, 2025. The recall affects the IV administration set labeled as 490426 with UDIs listed. The defect is potential backflow from secondary to primary IV containers and an inability to prime. Patients and healthcare providers should stop using these devices immediately and follow the manufacturer’s recall instructions.
B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow
B Braun Medical Inc. recalls 5,100 IV administration sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The recall cites backflow of medication from piggyback containers into primary IV containers and an occlusion that prevents priming. Patients should stop use immediately and follow recall instructions.
One unit of the Siemens MAMMOMAT Fusion operator table is recalled after being sold with a bus-installation kit. The device is not intended for bus installations and is designed for stationary operation. Health care providers should stop using the device immediately and follow the manufacturer’s recall 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.
Lifepro Fitness recalls Bioremedy Infrared Sauna Blankets sold with gray-faced controllers due to burn risk. The recall affects models LP-BRMDYL-BLK, LP-BRMDYL-GRY, LP-BRMDYR-BLK, LP-BRMDYR-GRY, LP-BRMDYR-BLU, LP-BRMDYR-PNK, and LP-BRMDYR-PRPL. Consumers should stop using and unplug the blankets and visit Lifepro’s recall page for a replacement.
Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.
M.C.I. Foods recalled 1,040 cases of ready-to-eat Egg and Cheese Breakfast Burritos and Wraps sold to seven distributors nationwide for institutional use. A cooked egg ingredient used in the ready-to-eat products tested positive for Listeria monocytogenes. Consumers should not consume the product and should contact M.C.I. Foods for refund or replacement; notification will be by letter.
Wilteexs recall 1-liter bioethanol fuel bottles imported by Wilteexs after safety-standard violations. The bottles lack flame mitigation devices and carry a false “Non Toxic” disclaimer. Consumers should stop using the recalled bottles and contact Wilteexs for a full refund.
Elixir by Coco March Mineral Sunscreen SPF 50 was recalled on 2025-10-10 and remains active. Manufactured or distributed by CA Botana International and distributed in several states. The FDA recall cites CGMP deviations as the hazard. Consumers and healthcare providers should stop using the product immediately and consult a healthcare provider for guidance.