Wheelchairs, Beds & Lifts recalls

172 medical device recalls in the wheelchairs, beds & lifts category are on file with the FDA, from 2012 to 12 Aug 2026. The leading reason is device malfunction.

Total recalls172since 2012
Last 12 months23reported
Class I2112% of total
Ongoing71latest 12 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 21 12%Class II 149 87%Class III 2 1%

Why wheelchairs, beds & lifts is recalled

By year

Ongoing wheelchairs, beds & lifts recalls

71 active

All wheelchairs, beds & lifts recalls, newest first

172 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIQuantum Rehab Quantum 4Front 2HD recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Q6 Edge recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum rehab Q6 Edge recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Q6 Edge recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab R-trak recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Quantum Rival recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Q6 Edge HD recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Quantum recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab 4Front recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIDrive and munevo Drive r-net Powered Wheelchair Hands-Free recalledMunevoDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Quantum 4Front recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Quantum Outback recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIQuantum Rehab Q6 Edge 3 Stretto recalled by Pride Mobility ProductsPride Mobility ProductsDevice MalfunctionNationwide
DeviceCLASS IIM5 Corpus Power Wheelchair recalled by PermobilPermobilOtherNationwide
DeviceCLASS IIM3 Corpus Power Wheelchair with Heavy Duty Shock recalled by PermobilPermobilPotency & AssayNationwide
DeviceCLASS IIPower F2 Powered Fastening System recalled by Ferno-WashingtonFerno-WashingtonOtherNationwide
DeviceCLASS IWhill Model F, with software versions before HMI: 2.23 / MC recalledWhillDevice MalfunctionKS
DeviceCLASS IIArjo Tenor mobile passive patient lift recalledArjohuntleigh Polska Sp. z.o.oDevice MalfunctionNationwide
DeviceCLASS IIRaz-AT (Attendant Tilt) Mobile Shower Commode Chair recalledRaz DesignOtherNationwide
DeviceCLASS IIMolift Mover recalled by Etac A/sEtacDevice MalfunctionNationwide
DeviceCLASS IIMolift 2-point sling bars (Accessory to mobile hoists) recalledEtacDevice MalfunctionNationwide
DeviceCLASS IIMolift 4-point sling bars (Accessory to mobile hoists) recalledEtacDevice MalfunctionNationwide
DeviceCLASS IMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalledMax MobilityOther44 states
DeviceCLASS IMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalledMax MobilityOther44 states
DeviceCLASS IMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalledMax MobilityOther44 states
DeviceCLASS IMulti Joystick R-net recalled by mo-Vis BVBAmo-Vis BvbaDevice MalfunctionNationwide
DeviceCLASS IIdm-multi-r. Electrical wheelchair component recalled by mo-Vis BVBAmo-Vis BvbaDevice MalfunctionNationwide
DeviceCLASS IAll-round Joystick R-net Light recalled by mo-Vis BVBAmo-Vis BvbaDevice MalfunctionNationwide
DeviceCLASS IIdm-arlite-r. Electrical wheelchair component recalled by mo-Vis BVBAmo-Vis BvbaDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.