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Drive R900RDRecalls & reported problems

Drive Devilbiss Healthcare · Rollator,8"4Whl.,Steel,Red,1/ea · 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 00822383548593), received between Feb 19, 2020 and Feb 19, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1

Patient problems

  • Fall1
  • Head Injury1

Recent adverse event reports

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

  • InjuryFeb 19, 2020Material Fragmentation; Material Fragmentation

    DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE DEVICE HAS NOT BE RETRIEVED FOR EVALUATION. THE END-USER WAS USING THE DEVICE TO GET TO THE REST ROOM AT APPROXIMATELY 1AM. THE LOOP PART ON THE BRAKE BROKE AND SHE FELL. SHE HIT HER HEAD AND WAS BLEEDING. SHE WENT TO THE HOSPITAL. SHE DOES NOT REMEMBER WHAT HAPPENED. AS OF THE CONVERSATION WITH POST MARKET SHE WAS STILL IN THE HOSPITAL. ACCORDING TO HER SPOUSE SHE HAS BEEN FALLING A LOT LATELY.

    Patient problems: Fall; Head Injury

    MAUDE report 9728559 ↗

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.