Go Chair MEDRecalls & 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. · Class 2
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00606509100250), received between Oct 26, 2022 and Mar 16, 2026 — classified as 9 injuries.
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 Available9
Patient problems
- Bruise/Contusion4
- Bone Fracture(s)3
- Abrasion1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE WAS ON A PUBLIC BUS IN (B)(6) WHEN THE DRIVER MADE VERY SHARP TURN AND USER WAS THROWN OVER THE RIGHT SIDE OF THE UNIT INTO OTHER PASSENGERS AND ONTO THE FLOOR. USER WAS RIDING IN A UNIT ON THE BUS NOT RATED FOR OCCUPIED TRANSIT.
Patient problems: Bruise/Contusion
MAUDE report 24604194 ↗InjuryDec 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHILE RIDING THE CHAIR IN HIS DRIVEWAY, WHICH HE EMPHASIZED IS NOT STEEP, THE CHAIR ALLEGEDLY TIPPED OVER.
Patient problems: Bruise/Contusion
MAUDE report 23837644 ↗InjurySep 4, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE GOT HER CLOTHING STUCK IN THE JOYSTICK AND THE CHAIR MOVED AND SHE ALLEGEDLY RAMMED HER RIGHT SHIN INTO THE DRESSER CAUSING OPEN CUTS AND HER LEFT FOOT ALLEGEDLY GOT CRUSHED.
Patient problems: Bruise/Contusion
MAUDE report 22966227 ↗InjuryAug 28, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S SON IN LAW ALLEGES CONSUMER HAS A MUSCLE DISORDER THAT AFFECTS HER ABILITY TO FEEL SO SHE COULD NOT FEEL PAIN THAT SHE WAS ALLEGEDLY GETTING FROM A SHARP AREA ON THE BACK AREA OF THE FOOTREST PLATE THAT ALLEGEDLY DUG INTO HER RIGHT FOOT AND GOT AN INFECTION.
Patient problems: Abrasion
MAUDE report 22911686 ↗InjuryAug 7, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HIS CHAIR TIPPED OVER WHEN HE WENT FROM HIS GARAGE TO SIDEWALK.
Patient problems: Bone Fracture(s)
MAUDE report 22739409 ↗InjuryJul 15, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES AS SHE WAS GETTING OFF THE UNIT, HER NIGHT GOWN GOT STUCK ON THE JOYSTICK. IT ALLEGEDLY THREW HER OUT OF THE UNIT AND KEPT GOING IN CIRCLES AND RUNNING HER OVER.
Patient problems: Bone Fracture(s)
MAUDE report 22511510 ↗InjuryNov 15, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THAT SHE HAS TIPPED OVER SEVERAL TIMES IN HER CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 20693504 ↗InjuryJan 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS AT HER CAR AND TRANSFERRING INTO THE CAR WHEN THE UNIT ALLEGEDLY TIPPED SIDEWAYS WITH THE CONSUMER IN IT. PROVIDER ALSO ALLEGES THERE WERE TWO OTHER TIMES THE CONSUMER WAS OUTSIDE AND THE UNIT ALLEGEDLY TIPPED OVER WITH THE CONSUMER IN IT.
Patient problems: Bruise/Contusion
MAUDE report 18579375 ↗InjuryOct 26, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE FELL OFF OF HIS UNIT AND ALLEGEDLY WAS ON HIS BACK FOR FOUR HOURS TRYING TO GET UP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15674848 ↗
Other Wheelchair, Powered devices
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- Permobil M3Permobil, Inc. · Wheelchair, Powered1 recall59 reports
- TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGInvacare Corporation · Wheelchair, powered2 recalls2 reports
- 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.