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DRIVEMEDICAL GV974RDRecalls & reported problems

Drive Devilbiss Healthcare · Rollators4-Wheel Alum Product Description: F22 Rollator, Standard, Red · 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 00822383964140), received between Jun 15, 2023 and Jun 15, 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

  • Fall1

Recent adverse event reports

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

  • InjuryJun 15, 2023Break; Break

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN END USER'S PHYSICAL THERAPIST, WHO REPORTED THAT THE "RIGHT FRONT TIRE'S BEARING CAME OUT AND THE TIRE DISLODGED FROM THE MOUNTING TRACK ON THE WALKER WHILE IN USE," AND THAT "AS A RESULT THE [END USER] FELL." THERE WAS NO REPORT OR MEDICAL TREATMENT ASSOCIATED WITH THE COMPLAINT. MULTIPLE ATTEMPTS WERE MADE TO RETRIEVE THE PRODUCT FOR INVESTIGATION, WITH NO RESPONSE. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

    Patient problems: Fall

    MAUDE report 17140159 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources and updates

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