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Drive GV974BK-TRecalls & reported problems

Drive Devilbiss Healthcare · Patriot F22 Rollator, Tall, Black · 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 00822383582221), received between Jul 25, 2019 and Jul 25, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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

  • Collapse1

Patient problems

  • Fracture, Arm1

Recent adverse event reports

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

  • InjuryJul 25, 2019Collapse; Collapse

    (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE PATIENT STILL HAS THE UNIT. IT IS NOT AVAILABLE CURRENTLY FOR EVALUATION. WE NAVE PHOTOS ON FILE. THE ENDUSER WAS COMING AROUND THE ROLLATOR FROM BACK TO FRONT TO SIT DOWN. HE ATTEMPTED TO SIT AND THE DEVICE AND IT COLLAPSED AND THE FRONT WHEEL FELL OFF. THE CONSUMER FELL HITTING HIS ELBOW AND HEAD. HE WAS TAKEN TO THE HOSPITAL WHERE HE WAS DIAGNOSED WITH A FRACTURED ELBOW. HE HAS A CAST. PATIENT IS BEING TREATED BY AN ORTHOPAEDIST AND RECEIVING PAIN MEDS. HE IS IN A CAST.

    Patient problems: Fracture, Arm

    MAUDE report 8827205 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

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