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Drive RTL10372BKRecalls & reported problems

Drive Devilbiss Healthcare · Cane,Offset,Gel Grip,Black,1/EA,6/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 00822383246451), received between May 15, 2020 and May 15, 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

Recent adverse event reports

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

  • InjuryMay 15, 2020Material Fragmentation; Material Fragmentation

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A CANE. CANE WAS NOT RETRIEVED FOR EVALUATION. CANE SNAPPED IN HALF WHILE IN USE. END-USER FELL AND BROKE HIS GLASSES.

    Patient problems: Fall

    MAUDE report 10063484 ↗

Other CANE devices

All CANE devices →

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