Invacare Suzhou
FDA adverse event reports naming Invacare Suzhou as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INVACARE SUZHOU.
- Total reports
- 4,329
- Deaths
- 10
- Injuries
- 34
- Malfunctions
- 4,269
Reports per year
6911
78912
2,66213
80514
324
125
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Wheelchair, PoweredITI1,597
- Lift, Patient, Non-Ac-PoweredFSA1,251
- Compressor, Air, PortableBTI1,038
- Generator, Oxygen, PortableCAW343
- Lift, Patient, Ac-PoweredFNG51
- Wheelchair, MechanicalIOR25
- Nebulizer (Direct Patient Interface)CAF10
- Walker, MechanicalITJ9
- Chair, With CastersINM2
- Transport, Patient, PoweredILK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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