DRIVEMEDICAL TR18Recalls & reported problems

Drive Devilbiss Healthcare · WenzeliteStrollers Product Description: Extension Rails,Trotter,1pr/bag · Class 1

All models of DRIVEMEDICAL (111)

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 00822383121499), received between Sep 13, 2019 and Sep 13, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

Material Fragmentation1

Patient problems

Injury1

Recent adverse event reports

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

InjurySep 13, 2019Material Fragmentation; Material Fragmentation
(B)(6) IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A TRANSPORT CHAIR. OUR CLAIMS DEPARTMENT IS AWAITING DATA REGARDING THE DEVICE AND THE INCIDENT. WE HAVE NOT RECEIVED THE DEVICE FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. THE DEVICE REPORTEDLY FELL APART WHILE IN USE. THE USER WAS INJURED. BASED ON THE SERIAL NUMBER THE DEVICE WAS APPROXIMATELY FOUR (4) YEARS OLD.
Patient problems: Injury
MAUDE report 9033980 ↗

Device details

UDI-DI	`00822383121499`
Brand	DRIVEMEDICAL
Model	TR18
Company	Drive Devilbiss Healthcare
Product code	KNO · ACCESSORIES, WHEELCHAIR
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	Oct 3, 2024

Device type (GMDN): Attendant-only-propelled wheelchair, non-bariatric

A non-powered wheeled mobility device with a seat designed to enable a healthcare provider/carer to transport a non-bariatric person without the full capacity to walk, typically over short distances and over smooth ground. Often referred to as a transport wheelchair, it is typically designed with four small wheels and includes rear-fitted handles for attendant control of the chair; it does not provide the occupant a mechanism for self-propulsion (it is not a push-rim wheelchair). It provides no function outside of wheeled mobilization.

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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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