Go ChairRecalls & 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
- 6
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00606509100007), received between Sep 15, 2017 and Mar 6, 2024 — classified as 5 injuries, 1 malfunction.
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 Available6
- No Apparent Adverse Event1
Patient problems
- Bruise/Contusion2
- Abrasion1
- Bone Fracture(s)1
- Injury1
- Laceration(s)1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryMar 6, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER WAS RIDING ON PUBLIC TRANSPORT WHEN THE BUS HIT A SPEEDBUMP AND THE CHAIR WAS THROWN A FEW INCHES IN THE AIR BEFORE DROPPING BACK DOWN.
Patient problems: Bruise/Contusion
MAUDE report 18848274 ↗InjuryMay 21, 2021No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available; No Apparent Adverse Event; Appropriate Device Problem Term/Code Not Available
ALLEGES DRIVING ALONG HIGHWAY 7 AND BAYVIEW AND ATTEMPTED TO PASS A PEDESTRIAN. WHEN ATTEMPTING TO MANEUVER THE TERRAIN, THE DEVICE ALLEGEDLY TIPPED BACKWARDS.
Patient problems: Bruise/Contusion; Laceration(s)
MAUDE report 11863074 ↗MalfunctionMay 20, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES A STRANGE ODOR WAS COMING FROM THE CHAIR WHEN THEY PLUGGED IN THE CHARGER. PROVIDER ALSO ALLEGES THE BATTERIES STARTED LEAKING.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10074701 ↗InjuryNov 22, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S FRIEND ALLEGES CONSUMER WAS GOING FROM THE BATHROOM TO ANOTHER ROOM WHEN HIS CHAIR GOT STUCK AS HE WAS TRYING TO TURN TO GET THROUGH THE DOORWAY. HE ALLEGEDLY ENDED UP TIPPING OVER.
Patient problems: Injury
MAUDE report 9362739 ↗InjuryAug 9, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER'S CHAIR STOPPED SUDDENLY AND HE ALLEGEDLY SLID FORWARD AND HIS RIGHT FOOT ALLEGEDLY BROKE THE WHEEL COVER AND WAS CAUGHT IN THE PLASTIC JAGGED PIECES.
Patient problems: Bone Fracture(s)
MAUDE report 8880119 ↗InjurySep 15, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMERS HUSBAND ALLEGES THAT CONSUMER WAS BACKING UP ON A TRAIN AND HIT FORWARD ON THE JOYSTICK BY MISTAKE. CHAIR ALLEGEDLY TOOK OFF CAUSING CONSUMER TO ALLEGEDLY HIT HER LEG ON A KNOB ON A TRAIN SEAT.
Patient problems: Abrasion
MAUDE report 6868819 ↗
Other Wheelchair, Powered devices
- SmartDrive® MX2+Max Mobility, LLC · Wheelchair, Powered858 reports
- 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.