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Drive 10226GRecalls & reported problems

Drive Devilbiss Healthcare · Walker,2TrigRel,Adult,w/5"Whls,Grey,4/CS · 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 00822383253336), received between Oct 12, 2019 and Oct 12, 2019 — 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

Recent adverse event reports

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

  • InjuryOct 12, 2019Material Fragmentation; Material Fragmentation

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WALKER. THE UNIT HAS NOT BEEN RETURNED FOR EVALUATION. WHILE USING THE WALKER IN THE REST ROOM THE LEG REPORTEDLY SNAPPED AROUND THE SCREW, THE END-USER FELL AND HIT HER HEAD AND SHOULDER. SHE WAS C ON THE DRESSER. SHE WAS TAKEN TO THE HOSPITAL, THEY X-RAYED HER FEMUR WHICH WAS THE INITIAL CAUSE FOR HER USE OF THE DEVICE. SHE WAS RELEASED FROM THE ER THE SAME DAY WITH INSTRUCTIONS TO TAKE TYLENOL.

    Patient problems: Fall

    MAUDE report 9183070 ↗

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.