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Drive RTL10310Recalls & reported problems

Drive Devilbiss Healthcare · QuadCane,Sm Base,BLK,Foam Grip,1EA,4/CS · Class 1

Data updated Oct 16, 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 00822383254050), received between Jun 1, 2021 and Jun 1, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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 16, 2026.

Most reported problems

Device problems

  • Fracture1

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.

  • InjuryJun 1, 2021Fracture; Fracture

    (B)(4) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A CANE. WE HAVE NOT RECEIVED THE DEVICE FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVER ABUNDANCE OF CAUTION. WE WILL FILE A FOLLOW UP WHEN ADDITIONAL DATA BECOMES KNOWN. END-USER REPORTED THAT THE CANE BROKE IN HALF CAUSING HIM TO FALL DOWN 3 STAIRS HITTING HIS HEAD AND HURTING BACK. WE ARE AWAITING CONFIRMATION OF MEDICAL SERVICE.

    Patient problems: Fall; Head Injury

    MAUDE report 11917025 ↗

Other CANE devices

All CANE devices →

Sources and updates

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