Invacare Rehabilitation Equip
FDA adverse event reports naming Invacare Rehabilitation Equip as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INVACARE REHABILITATION EQUIP.
- Total reports
- 3,036
- Deaths
- 1
- Injuries
- 16
- Malfunctions
- 3,011
Reports per year
2,35814
67815
Source: FDA adverse event reports by year received, 2014–2015. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Generator, Oxygen, PortableCAW1,573
- Wheelchair, PoweredITI798
- Lift, Patient, Non-Ac-PoweredFSA467
- Compressor, Air, PortableBTI182
- Wheelchair, MechanicalIOR9
- Walker, MechanicalITJ2
- Nebulizer (Direct Patient Interface)CAF1
- Bed, Ac-Powered Adjustable HospitalFNL1
- Adaptor, HygieneILS1
- Vehicle, Motorized 3-WheeledINI1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Invacare Rehabilitation Equip automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.