Invacare Rehabilitation Equipment Co.
FDA adverse event reports naming Invacare Rehabilitation Equipment Co. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INVACARE REHABILITATION EQUIPMENT CO..
- Total reports
- 2,068
- Deaths
- 4
- Injuries
- 22
- Malfunctions
- 2,035
Reports per year
1,45215
60416
1217
Source: FDA adverse event reports by year received, 2015–2017. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Wheelchair, PoweredITI725
- Lift, Patient, Non-Ac-PoweredFSA670
- Generator, Oxygen, PortableCAW498
- Compressor, Air, PortableBTI150
- Wheelchair, MechanicalIOR18
- Walker, MechanicalITJ3
- Bed, Ac-Powered Adjustable HospitalFNL1
- Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY1
- Footrest, WheelchairIMM1
- Cushion, WheelchairIMP1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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