243 recalls tagged with “tip over risk”.
B Braun Medical Inc. recalls 190,625 IV administration sets worldwide, including US and Canada, for risk of backflow from secondary to primary IV containers and occlusion that prevents priming. The recall affects BBMI’s Infusomat Space, Outlook Pump, and Vista Basic Pump compatible sets. Stop-use immediately and follow recall instructions.
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.
B Braun Medical Inc recalled 13,600 extension set units used with Infusomat Space and related pumps sold through multiple healthcare distributors worldwide. The recall cites a backflow risk from secondary piggyback containers into primary IV containers and an inability to prime due to occlusion. Healthcare providers and facilities should stop using the device immediately and follow manufacturer-re
B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.
BBraun Medical recalled 12,700 ADDitIV gravity IV sets distributed worldwide. The sets can backflow medication from piggyback containers into primary IV containers and cannot be primed. Healthcare providers and patients should stop using the sets immediately and follow the recall instructions from BBraun Medical.
Siemens Medical Solutions USA recalls the MAMMOMAT Inspiration operator table. The recall covers six units worldwide, including three in the United States. The operator table was sold with a bus-installation kit and is not designed or released for bus installations. Stop using the device immediately and contact Siemens for instructions.
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.
Bealife recalled its 5-Drawer Dressers on Oct. 23, 2025. The dressers are white and measure 32 inches high, 28 inches wide, and 16 inches deep. The model AP23-W is printed on packaging but not on the dresser itself. Consumers should stop using unanchored dressers and seek a full refund.
WLIVE recalled its Fabric 12-Drawer Dressers sold on Amazon after identifying a serious tip-over and entrapment hazard. The dressers are unstable if not anchored to the wall, violating the mandatory standard for clothing storage units under the STURDY Act. Consumers should stop using the recalled dressers immediately and contact WLIVE for a full refund.
Yamaha recalls 2021-2025 Drive 2 PTV golf cars sold by Yamaha dealers nationwide between June 2020 and July 2025. The recalled golf cars lack stop lights, creating a crash hazard that could result in serious injury or death. Owners should stop using the recalled golf car immediately and contact an authorized Yamaha Golf Car dealer for a free installation of two stoplights.
AOWOS recalled approximately 42,000 12-drawer dressers sold on Walmart.com due to a tip-over hazard. The dressers lack stability if not anchored to the wall, posing serious risks of injury or death to children. Consumers should stop using the dressers immediately and contact AOWOS for a full refund.
RH recalled Byron tables and desks sold at RH Galleries and outlets and on RH.com from November 2023 through July 2025. The recall covers 31 SKUs across three models with stone and marble tops and wood legs. The recalled furniture can collapse if a gap forms between the leg and tabletop and a horizontal force is applied. Consumers should stop using recalled units and contact RH for a full refund,,
ESR HaloLock wireless power banks were recalled in an expansion that now includes model 2G505. The recall covers models 2G520, 2G505B and 2G512B previously recalled and adds 2G505. The recall is distributed by Waymeet. The lithium-ion batteries can overheat and ignite. Consumers should stop using recalled power banks and seek a full refund from Waymeet.
Mom Genius recalled retractable safety gates due to entrapment risk that can cause serious injury or death. The recall covers gates with a retractable mesh screen in black and gray. The model is SH.20.006B02. Consumers should stop using the gate and seek a full refund.
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.
Coca-Cola Southwest Beverages recalled 791 Sprite 12oz cans sold at retailers in Texas after metal fragments were found in the product. The recall concerns Sprite 12oz cans in 35-pack and 12-pack formats. Consumers should not drink the product and should contact Coca-Cola Southwest Beverages LLC by email for refunds or replacements.
Gunaito recalled 10-drawer dressers sold on Walmart.com after reports of tip-over and entrapment hazards. The recall targets brown and white dressers with model numbers HD006BN-SLCD and HD006WH-SLCD. The product packaging bears the codes HD006BN-SLCD or HD006WH-SLCD.
Zyntony recalled Kogalla power banks sold on Kogalla.com due to fire and burn hazards. The recall targets BP125, BatPak 2F and BatPak 3F models. The lithium-ion batteries can overheat and ignite, even when not in use. Consumers should stop using the recalled power banks and contact Kogalla for a free replacement.
Abiomed recalled 10,153 Automated Impella Controllers and related components due to potential cybersecurity vulnerabilities in the operating system. The recall spans multiple international product codes and was first issued for devices distributed nationwide and internationally. Providers should stop using the affected controllers and follow manufacturer instructions immediately.
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.