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DRIVEMEDICAL 146-R726BLRecalls & reported problems

Drive Devilbiss Healthcare · Rollators4-Wheel Alum Product Description: Rollator,6in4Whl.Alum.PaddedSt,Blue,1/c · Class 1

All models of DRIVEMEDICAL (111)

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 00612479223103), received between May 1, 2023 and May 1, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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

  • Improper or Incorrect Procedure or Method1

Patient problems

  • Fall1

Recent adverse event reports

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

  • InjuryMay 1, 2023Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT INVOLVING A ROLLATOR BY A PROVIDER, WHO STATED THAT "THE WALKER WAS TOO LARGE FOR THE PATIENT AND SHE FELL USING IT. WAS ALLEGEDLY INJURED AND HOSPITALIZED." THERE WERE NO DETAILS ON THE TYPE OR SEVERITY OF THE INJURY WITHIN THE INITIAL COMPLAINT. DRIVE IS CONTINUING TO TRY TO CONTACT THE END USER FOR ADDITIONAL INFORMATION AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Fall

    MAUDE report 16847521 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources and updates

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