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DRIVEMEDICAL 146-R726SLRecalls & reported problems

Drive Devilbiss Healthcare · Rollators4-Wheel Alum Product Description: Rollator,6'4Whl.Alum.PaddedSt,Slvr,1/cs · 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 00612479223134), received between Apr 11, 2023 and Apr 11, 2023 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryApr 11, 2023Break; Break

    (B)(6) HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY A HEALTHCARE PROVIDER, WHO STATED THAT "WHEEL AND BACKREST BROKE, AND THE END USER SUFFERED AN INJURY." 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: Insufficient Information

    MAUDE report 16717961 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources and updates

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