Drive KA1200-2GKBRecalls & reported problems

Drive Devilbiss Healthcare · Nimbo Walker, XS, Knight Blue · Class 1

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 00822383583815), received between May 26, 2023 and May 26, 2023 — classified as 1 injury.

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

Appropriate Device Problem Term/Code Not Available1

Patient problems

Bruise/Contusion1
Fall1
Swelling/ Edema1

Recent adverse event reports

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

InjuryMay 26, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF A COMPLAINT REGARDING A PEDIATRIC POSTERIOR WALKER BY AN END USER'S MOTHER, WHO STATED THAT "THE WHEELS LOCKED IN THE FRONT," CAUSING HER SON TO FALL AND THE WALKER TO FALL ON TOP OF HIM, RESULTING IN "A LARGE GOOSE EGG ON HIS FOREHEAD." THE END USER DID NOT RECEIVE MEDICAL TREATMENT AND THE INJURY RESOLVED IN 4 DAYS. 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: Bruise/Contusion; Fall; Swelling/ Edema
MAUDE report 17011305 ↗

Device details

UDI-DI	`00822383583815`
Brand	Drive
Model	KA1200-2GKB
Company	Drive Devilbiss Healthcare
Product code	ITJ · WALKER, 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	Nov 17, 2023

Device type (GMDN): Handgrip disability-assistive walker, non-powered, non-foldable

A non-powered, all- or partially-wheeled mobility aid in the form of a waist- or trunk-high, non-foldable framework with handgrips or hand-held frame and three or four legs, designed to provide a stable support for a patient with a walking disability, a geriatric, obese, or infirm patient when standing or ambulating; it might be used for rehabilitation. It is constructed of lightweight metal, plastic, and rubber materials in the shape of a mobile support structure which the patient holds and pushes in front of them as they walk. It is non-foldable and may include a braking mechanism; it may be width-adjustable and some types may include a seat on which the patient can rest.

Other WALKER, MECHANICAL devices

Drive 10257BL-1
Drive Devilbiss Healthcare · WALKER, MECHANICAL
13 reports
Drive R726RD
Drive Devilbiss Healthcare · WALKER, MECHANICAL
1 death10 reports
Drive 790
Drive Devilbiss Healthcare · WALKER, MECHANICAL
10 reports
Drive R728BL
Drive Devilbiss Healthcare · WALKER, MECHANICAL
9 reports
Drive 10257RD-1
Drive Devilbiss Healthcare · WALKER, MECHANICAL
9 reports
DRIVEMEDICAL 795B
Drive Devilbiss Healthcare · WALKER, MECHANICAL
9 reports
Drive R726BK
Drive Devilbiss Healthcare · WALKER, MECHANICAL
9 reports
Drive 10215BL-1
Drive Devilbiss Healthcare · WALKER, MECHANICAL
8 reports

All WALKER, 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