DRIVEMEDICAL RTL10353Recalls & reported problems

Drive Devilbiss Healthcare · Canes & CrutchesAccessories Product Description: Quad Tip, 1 blister, 10/CV · Class 1

All models of DRIVEMEDICAL (111)

Data updated Oct 18, 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 00822383545059), received between Aug 14, 2025 and Aug 14, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Material Integrity Problem” (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 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Material Integrity Problem1

Patient problems

Hip Fracture1

Recent adverse event reports

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

InjuryAug 14, 2025Material Integrity Problem; Material Integrity Problem
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A CANE TIP BY THE PROVIDER, WHO STATED THAT DURING USE ON A HARDWOOD FLOOR OF THEIR HOME, THE END USER FELL AND BROKE HER HIP, REQUIRING HOSPITALIZATION. THE PROVIDER REPORTED THAT THE BOTTOM OF THE CANE TIP DOES NOT GRIP TO THE HARD FLOOR SURFACE DURING USE. 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: Hip Fracture
MAUDE report 22804336 ↗

Device details

UDI-DI	`00822383545059`
Brand	DRIVEMEDICAL
Model	RTL10353
Company	Drive Devilbiss Healthcare
Product code	INP · TIPS AND PADS, CANE, CRUTCH AND WALKER
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jul 15, 2019

Device type (GMDN): Walking aid tip

A device designed as a formed piece of non-slip material (e.g., rubber or suitable plastic) that is attached to the ground-contacting end of a walking aid (e.g., a walking stick, crutch, or walking frame) to promote a secure purchase to the contact surface (ground or floor surfaces) thereby increasing the safety factor. This is a reusable device.

Other TIPS AND PADS, CANE, CRUTCH AND WALKER devices

DRIVEMEDICAL RTL10365-ADJ
Drive Devilbiss Healthcare · TIPS AND PADS, CANE, CRUTCH AND WALKER
6 reports
Walgreens 404722
Drive Devilbiss Healthcare · TIPS AND PADS, CANE, CRUTCH AND WALKER
1 report

All TIPS AND PADS, CANE, CRUTCH AND WALKER devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page