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DRIVEMEDICAL ATC19-BLRecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairTransport Chairs Product Description: Transport Chair,Alum.19in Blue,1/cs · Class 1

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00822383133621), received between Jul 11, 2022 and Oct 6, 2022 — classified as 3 injuries.

The most frequently reported specific device problem is “Material Integrity Problem” (2 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, 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

  • Material Integrity Problem2
  • Fracture1

Patient problems

  • Bone Fracture(s)1
  • Bruise/Contusion1
  • Fall1
  • Hematoma1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 6, 2022Material Integrity Problem; Material Integrity Problem

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY AN END USER, WHO STATED THAT "THE BACK OF IT BROKE OFF RIGHT STRAIGHT ACROSS BOTH SIDES," CAUSING HER TO FALL BACKWARDS AND LAND ON THE FLOOR. SHE REPORTED SUSTAINING SOME BRUISES ON HER HIPS, AND THAT "HER WHOLE BODY WAS STRESSED." SHE USED HER LIFE ALERT DEVICE TO OBTAIN MEDICAL ATTENTION, AND WAS IN THE HOSPITAL FOR 6 DAYS, HOWEVER, DID NOT SUSTAIN ANY INJURIES BESIDES THE BRUISING. 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: Fall

    MAUDE report 15553399 ↗
  • InjurySep 20, 2022Material Integrity Problem; Material Integrity Problem

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN ATTORNEY, WHO REPORTED THAT "THE END USER WAS SEATED IN A TRANSPORT CHAIR WHEN IT COLLAPSED DUE TO A WELD BREAK CAUSING HIM TO FALL AND FRACTURE HIS LEFT SCAPULA." 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: Bone Fracture(s)

    MAUDE report 15455272 ↗
  • InjuryJul 11, 2022Fracture; Fracture

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR. THE END USER'S DAUGHTER REPORTED THAT WHILE "I WAS WHEELING MY MOTHER ON THE STREET, THE CHAIR BROKE WITH HER IN IT. THE METAL BAR HOLDING THE FRONT WHEEL IN PLACE BROKE IN HALF, CAUSING THE CHAIR TO COLLAPSE" BENEATH HER. THE END USER "FELL ON THE SIDEWALK AND HIT HER HEAD." THE END USER "SUFFERED BRUISING ON HER HEAD, A CONTUSION, SOFT TISSUE SWELLING AND HEMATOMA ON HER FOREHEAD AND EYE AND NEEDED A CT SCAN." DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT.

    Patient problems: Bruise/Contusion; Hematoma

    MAUDE report 14977764 ↗

Other Wheelchair, mechanical devices

All Wheelchair, mechanical devices →

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