R-TRAKRecalls & 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
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00606509200226), received between Jan 25, 2024 and Jul 30, 2026 — classified as 5 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 Available5
Patient problems
- Bruise/Contusion2
- Abrasion1
- Bone Fracture(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJul 30, 2026Appropriate Device Problem Term/Code Not Available
Provider states consumer was in a crosswalk when they were struck by an automobile. The chair turned over and is damaged.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50081568 ↗InjuryJun 15, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER'S CARE GIVER ALLEGES THE WHEELS WERE SPINNING INCESSANTLY ON UNIT THEN CAUGHT TRACTION AND GOT THROWN DOWN THE FRONT PORCH STEPS WITH USER IN IT. ALLEGES THE UNIT THREW THE USER OUT OF THE CHAIR ONTO CEMENT PACERS ON THE GROUND. THEY ALSO ALLEGE THEY HAVE BEEN HAVING ISSUES WITH PRODUCT EVER SINCE IT WAS RECEIVED, AND DEALER HAS EITHER BEEN HARD TO GET A HOLD OF OR DOES NOT ANSWER FOR WEEKS.
Patient problems: Bruise/Contusion
MAUDE report 25499691 ↗InjuryJun 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER IS SITTING WAY TO FAR FORWARD. OVERALL LENGTH WITH SEATING SHE CAN'T GET IN AND OUT OF HER VAN. CONSUMER ALLEGEDLY BROKE THREE TOES DUE TO THE CASTER SWING AND RESISTANCE WHEN TRYING TO MANEUVER IN TIGHT SPACES. THERE IS NO WAT TO GET HER BACK ANY FURTHER AT BEST AN INCH. DUE TO THE SHORT SEAT.
Patient problems: Bone Fracture(s)
MAUDE report 22282448 ↗InjuryDec 19, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES THE CHAIR CONTINUED TO DRIVE WHILE GOING THRU HER FRONT DOOR AFTER SHE RELEASED THE JOYSTICK ALLEGEDLY CAUSING HER TO CRASH INTO THE DOOR FRAME.
Patient problems: Bruise/Contusion
MAUDE report 20975827 ↗InjuryJan 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE UNIT HAS LARGE AIRPLANE TIRES ON THE FRONT WHICH ALLEGEDLY DIDN'T TURN/GUIDE JUST FACED EACH OTHER AND ALLEGEDLY WHIPPED BACK & FORTH SLAMMING INTO EVERYTHING IN THE HOUSE ON #1 GEAR SPEED..(LOWEST) ¿AT ONE POINT THE UNIT SUDDENLY PINNED THE CONSUMER'S LEFT HAND BETWEEN IT'S METAL AND A SHARP CORNER OF A CABINET.
Patient problems: Abrasion
MAUDE report 18579367 ↗
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.