DRIVEMEDICAL K320DDA-ELRRecalls & reported problems

Drive Devilbiss Healthcare · Transport/WheelchairWheelchairs K3 Product Description: Cruiser III,20"Lt.Wt,FlipBk,DskArm,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 00822383123387), received between Sep 17, 2020 and Sep 17, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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

Device Slipped1

Patient problems

Bone Fracture(s)1
Fall1

Recent adverse event reports

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

InjurySep 17, 2020Device Slipped; Device Slipped
DRIVE DEVILBISS IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. WE HAVE NOT RECEIVED THE DEVICE FOR EVALUATION. A REPLACEMENT WAS SENT TO THE CUSTOMER. THE USER WAS GETTING UP ONE NIGHT TO GO TO THE BATHROOM. SHE HELD ONTO THE WHEELCHAIR AND IT ROLLED OUT BEHIND HER. SHE FELL AND FRACTURED HER FEMUR. SHE CONTINUED TO USE THE DEVICE. IT ROLLED OUT UNDER HER AGAIN, SHE FELL, BROKE HER HIP DOING REHAB.
Patient problems: Bone Fracture(s); Fall
MAUDE report 10548146 ↗

Device details

UDI-DI	`00822383123387`
Brand	DRIVEMEDICAL
Model	K320DDA-ELR
Company	Drive Devilbiss Healthcare
Product code	IOR · Wheelchair, mechanical
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	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.

Other Wheelchair, mechanical devices

MEDLINE K1186N22S
Medline Industries, Inc. · Wheelchair, mechanical
48 reports
Guardian K4186N24E
Medline Industries, Inc. · Wheelchair, mechanical
22 reports
MEDLINE INDUSTRIES, INC. MDS808650
Medline Industries, Inc. · Wheelchair, mechanical
18 reports
Medline MDS806850
Medline Industries, Inc. · Wheelchair, mechanical
17 reports
Quickie 7 Series
Sunrise Medical (US) LLC · Wheelchair, Mechanical
1 death10 reports
Guardian K3186N24E
Medline Industries, Inc. · Wheelchair, mechanical
10 reports
Guardian K3206N24S
Medline Industries, Inc. · Wheelchair, mechanical
9 reports
MEDLINE K3186N34S
Medline Industries, Inc. · Wheelchair, mechanical
9 reports

All Wheelchair, 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