Drive RTL10342Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383246574), received between Dec 4, 2024 and Dec 4, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Material Twisted/Bent” (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

Recent adverse event reports

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

• InjuryDec 4, 2024Material Twisted/Bent; Material Twisted/Bent

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A CANE BY THE END USER WHO REPORTED THAT THE CANE BENT WHILE IN USE, CAUSING HIM TO FALL AND BREAK HIS WRIST, FOR WHICH HE WAS PRESCRIBED A BRACE AND PHYSICAL THERAPY. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

  Patient problems: Bone Fracture(s); Limb Fracture

  MAUDE report 20844445 ↗