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Drive RTLFW19RW-RDRecalls & reported problems

Drive Devilbiss Healthcare · Flyweight,19in Rem Whls,Red,RTL,1 EA · Class 1

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 00822383246413), received between Nov 17, 2022 and Nov 17, 2022 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Head Injury1
  • Neck Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 17, 2022Break; Break

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY AN END USER'S SON, WHO STATED "SHE LEANED BACK, THE BACK GAVE WAY AND THE ROD SNAPPED. SHE FELL AND HIT THEIR HEAD." THERE WAS NO REPORT OF MEDICAL TREATMENT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Head Injury; Neck Pain

    MAUDE report 15812597 ↗

Other Wheelchair, mechanical devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.