DRIVEMEDICAL ATC17-BKRecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairTransport Chairs Product Description: Transport Chair17" Black,1/cs · 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 00822383133638), received between Jul 20, 2023 and Jul 20, 2023 — 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 18, 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.

InjuryJul 20, 2023Fracture; Fracture
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A TRANSPORT CHAIR BY AN END USER'S DAUGHTER, WHO STATED THAT "THE FRAME BROKE AND [THE END USER] FELL AND HIT HER HEAD." THE END USER WAS REPORTEDLY TAKEN TO THE EMERGENCY ROOM, BUT NO ADDITIONAL DETAILS WERE PROVIDED REGARDING THE DETAILS OF HER MEDICAL TREATMENT. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.
Patient problems: Fall; Head Injury
MAUDE report 17361209 ↗

Device details

UDI-DI	`00822383133638`
Brand	DRIVEMEDICAL
Model	ATC17-BK
Company	Drive Devilbiss Healthcare
Product code	INN · CHAIR, ADJUSTABLE, MECHANICAL
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 7, 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.

Other CHAIR, ADJUSTABLE, MECHANICAL devices

Prime TC 1460-000-000
Stryker Corporation · CHAIR, ADJUSTABLE, MECHANICAL
1 recall107 reports
Raz Raz-AP
Raz Design Inc · Chair, Adjustable, Mechanical
1 recall0 reports
Raz Raz-AT
Raz Design Inc · Chair, Adjustable, Mechanical
1 recall0 reports
Raz Raz-ART
Raz Design Inc · Chair, Adjustable, Mechanical
1 recall0 reports
Raz Raz-AT600
Raz Design Inc · Chair, Adjustable, Mechanical
1 recall0 reports
Aquatec Ocean -VIP Kit Series 1470000
Invacare Corporation · CHAIR, ADJUSTABLE, MECHANICAL
1 death3 reports
Raz Raz-CAT
Raz Design Inc · Chair, Adjustable, Mechanical
2 reports
Staxi ST010
Three Bears(Jiangsu)Healthcare Technology CO.,Ltd · Chair, Adjustable, Mechanical
1 report

All CHAIR, ADJUSTABLE, MECHANICAL 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