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Quickie Mid-Wheel Drive Power WheelchairRecalls & reported problems across all models

Sunrise Medical (US) LLC · 2 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
44
Deaths reported
3
Injuries reported
37
Recalls
0

We found 2 models of Quickie Mid-Wheel Drive Power Wheelchair by Sunrise Medical (US) LLC in the FDA's device registry (GUDID). Together they are named in 44 adverse event reports in the FDA's MAUDE database, received between Aug 10, 2017 and Jan 14, 2020 — classified as 3 deaths, 37 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (9 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported Quickie Mid-Wheel Drive Power Wheelchair problems

Device problems

  • Adverse Event Without Identified Device or Use Problem12
  • Unintended Movement9
  • Break5
  • Device Fell3
  • Mechanical Problem3
  • Detachment of Device or Device Component2
  • Insufficient Device Problem Information2
  • Unintended Collision2

Patient problems

  • Fall24
  • Bone Fracture(s)18
  • Injury11
  • Bruise/Contusion4
  • Death3
  • Concussion2
  • Head Injury2
  • Joint Dislocation2

Quickie Mid-Wheel Drive Power Wheelchair models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent Quickie Mid-Wheel Drive Power Wheelchair adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page