Invacare® AVIVA FX Power Wheelchair IFX-20MPRecalls & reported problems
Invacare Corporation · Invacare® AVIVA FX Power Wheelchair · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Nov 12, 2021Open, Classified
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury
Z-0446-2022 · Root cause: Software design · FDA record ↗
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- TDX SP2 with LiNX Electronics TDXSP2Invacare Corporation · Wheelchair, powered2 recalls0 reports
- Invacare® TDX SP2 with Captain's Seat TDXSP2VInvacare Corporation · Wheelchair, powered2 recalls0 reports
- Q6 Edge 3Pride Mobility Products Corp · Wheelchair, Powered4 deaths86 reports
- Q6 Edge 2.0 Q6 Edge 2.0 / Q6 Edge 2.0 with iLevelPride Mobility Products Corp · Wheelchair, Powered1 death83 reports
- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.