Quickie® Rear Wheel Drive Power Wheelchair EIS62Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05022408044252), received between Nov 6, 2017 and Nov 17, 2017 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Self-Activation or Keying” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 17, 2017Self-Activation or Keying; Therapeutic or Diagnostic Output Failure

  PLEASE SEE INITIAL MDR 2937137-2017-00016.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7043547 ↗
• InjuryNov 6, 2017Unintended Collision

  SUNRISE MEDICAL (US) LLC RECEIVED A COURT SUMMONS ON (B)(4) 2016 REGARDING AN INCIDENT POSSIBLY INVOLVING AN (B)(4) SC POWER WHEELCHAIR. THE SUMMONS STATES THAT ON (B)(6) 2016, END USER WAS A PASSENGER IN A CUSTOM-MADE VAN OPERATED BY HER FATHER. THE END USER'S CHAIR, WHICH THE SUMMONS STATES IS AN (B)(4) SE WAS SECURED IN THE REAR OF THE CUSTOM MADE VAN WHICH WAS INVOLVED IN A MOTOR VEHICLE COLLISION. IT IS ALLEGED IN THE SUMMONS THAT AS A RESULT OF THE COLLISION, THE D-RING DESIGNED TO SECURE THE SEATBELT IN PLACE FAILED, CAUSING THE END USER TO BECOME EJECTED FROM HER CHAIR AND SUFFER SERIOUS INJURIES.

  Patient problems: Injury

  MAUDE report 7004827 ↗