GoChairMED LiRecalls & reported problems
Pride Mobility Products Corp · A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. The GoChairMED Li has an upgrade to the battery (lithium), add memory foam with soft touch cover, and modify the anti tip location. · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00606509100335), received between Feb 20, 2026 and Feb 20, 2026 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 20, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHILE DRIVING ON A SIDEWALK TOWARD A RAMP, THE UNIT ALLEGEDLY FLIPPED AS HE ATTEMPTED TO GO UP THE INCLINE AND LANDED ON TOP OF HIM.
Patient problems: Bruise/Contusion
MAUDE report 24399786 ↗
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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
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- 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.