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 during the 2026 MAUDE-to-AEMS transition 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.
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