102 recalls tagged with “fall hazard”.
BMW recalls 2025-2026 X1 and X2 models plus MINI Cooper and Countryman variants for front seat belt retractors with damaged torsion bars. The defect may fail to restrain occupants in a crash. Dealers will replace both front retractors at no cost. Owner letters begin November 7, 2025. VIN lookup will be available on NHTSA.gov the same day.
SEGMART recalled 55" mini round toddler trampolines with enclosure nets due to a strangulation risk from hammock, punching bag and hand ring accessories. Models SOSTT051BR, SOSTT051CR and SOSTT051YP are included. Trampolines without the accessory kits are not recalled. Consumers should stop using immediately and return for a full refund.
Fun and Function recalled MW7661 multi-point swing frames due to crack and break risk. The frames were sold online by Funandfunction.com from May 2022 through February 2026 for $200-$250. Consumers should stop using the product immediately and contact the company for a full refund.
Head USA recalls ski boots with fluorescent yellow components from 2016–2022 model years. The recall covers boots and inserts with six-digit article codes. Consumers should stop using recalled boots immediately and contact Head for a free replacement or sole-insert option.
Samson International is recalling Bellevue and Oaklynn canopy bed frames sold under the Universal Broadmoor brand. The canopy beams can collapse when the bed is moved, posing an impact and injury risk. Stop using the bed immediately and contact Samson for a free repair kit that includes four mounting brackets and hardware.
OCUN NA recalled Condor HMS Triple Carabiners sold online and through climbing retailers after the gate may fail to close automatically. The carabiner features an independent internal wire gate and a triple locking action. Stop using the recalled carabiner immediately and contact OCUN NA for a free replacement.
AirClub recalled convertible bassinets that convert into bedside sleepers due to a hazardous attachment mechanism. The recall affects models labeled QX-831. The defect creates an opening between the bedside sleeper and mattress, posing a risk of serious injury or death to infants. Stop using the product immediately and contact AirClub for a replacement attachment mechanism.
Petzl America recalls Nomic and Ergonomic ice climbing axes due to a shaft break risk that could cause a fatal fall. The recall involves specific serial ranges across two models and targets accessories sold through specialty retailers and online shops. Consumers should stop using the axes and pursue a free repair kit from Petzl America.
Fagron Compounding Services recalled 34,260 bags of Vancomycin HCI Injection across the United States. The recall cites lack of sterility assurance and a blue Break-Off-Part that could detach from the administration port. Healthcare providers and patients should stop using the product immediately and follow manufacturer guidance.
Aisstxoer adult bicycle helmets sold on Amazon by YXTDZ Store are being recalled. The helmets fail to meet mandatory safety standards for impact attenuation and stability, creating a serious head-injury risk. Stop using the recalled helmet now and contact YXTDZ Store for a full refund; destroy the helmet and email a photo to yxtdzamz@126.com.
Goregent is recalling Goregent-branded infant walkers sold on Amazon. The recalled walkers can fit through a standard doorway and fail to stop at the edge of a step. Parents should stop using the recalled walkers immediately and contact Goregent Official Store for a full refund.
Tainoki Fine Furniture recalled three office chairs sold at HomeGoods stores nationwide from August 2025 through December 2025 for about $180 to $200. The base can bend, creating a fall hazard. Stop using the chairs immediately and follow the recall instructions on the company site for a full refund.
Specialized recalled all Turbo Como SL electric bicycles sold online at specialized.com and through Authorized Specialized Retailers. A fatigue crack in the fork steerer tube can cause progressive fork failure and a fall. Owners should stop riding immediately and arrange a free fork replacement at an Authorized Dealer; replacement parts are expected in Spring 2026.
LFTE USA recalled Playground Swing Set Seats on March 12, 2026. The swing seats pose a fall hazard due to potential rivet failure. The recall affects model number 999604 with the code 'LF-65708' marked on the seat pad.
Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set after lots were labeled with expiration dates that exceed true shelf life. The recall affects two reference parts with multiple UDI and lot numbers. Healthcare facilities should stop use and follow recall instructions.
Cook Medical recalled 49 units of the Approach CTO-12 Micro Wire Guide due to expiration dates that exceed the true shelf life. The recall covers two reference part numbers and multiple lots distributed worldwide. Healthcare providers and patients should stop using the affected devices immediately. Follow the manufacturer’s recall instructions or contact a healthcare provider for guidance.
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.
Andersen Windows recalled window opening control devices on February 26, 2026. The recall affects devices sold individually or installed on 100 Series casement windows manufactured before November 19, 2025. These devices pose fall and serious injury hazards due to the potential for detachment.
Bicystar recalled children's high chairs on February 26, 2026, due to serious fall and entrapment hazards. The affected high chairs lack required crotch restraints, putting children at risk. Consumers should stop using these chairs immediately and seek a refund.
Stryker Communications recalled 6,170 CHROMOPHARE Softlit Ring Surgical Light Systems distributed worldwide after confirming the ceiling cover weight may not be adequately supported. Hospitals should stop using the device immediately and follow recall instructions from the manufacturer. The recall is classified as Class II and is active as of February 23, 2026.