Quickie® Rear Wheel Drive Power Wheelchair EIPW2Recalls & reported problems
Sunrise Medical (US) LLC · P222 SE Power Wheelchair · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 05022408043415), received between Jan 2, 2020 and Jan 2, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 2, 2020Break
PER THE DEALER, (B)(6), HE PERFORMED AN EVALUATION OF THE CHAIR ON (B)(6) AND REPORTED THAT THE CHAIR WAS INVOLVED IN A CAR ACCIDENT PREVIOUS TO THAT EVALUATION. THE END USER WAS IN THE CHAIR WHEN THE CHAIR WAS HIT BY A CAR. THE PATIENT WAS DRAGGED BY THE CAR AND WAS HOSPITALIZED. THE EXTENT OF THE END USER'S INJURIES IS UNKNOWN.
Patient problems: Injury
MAUDE report 9539661 ↗
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- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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