Walgreens 404722Recalls & reported problems

Drive Devilbiss Healthcare · WALG WALKER FOLDING WITH WHEELS · Class 1

Data updated Oct 13, 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 10311917221066), received between Jul 17, 2024 and Jul 17, 2024 — 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

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

Most reported problems

Device problems

Appropriate Device Problem Term/Code Not Available1

Patient problems

Laceration(s)1

Recent adverse event reports

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

InjuryJul 17, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A WALKER BY THE END USER'S HUSBAND WHO STATED THAT HIS WIFE "SWUNG" THE WALKER AROUND AND HIT HER LEG WITH THE GLIDE SKI RESULTING IN A LACERATION. THE END USER RECEIVED MEDICAL TREATMENT FOR THE LACERATION AND WAS PRESCRIBED ANTIBIOTICS. 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: Laceration(s)
MAUDE report 19763896 ↗

Device details

UDI-DI	`10311917221066`
Brand	Walgreens
Model	404722
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	OTC
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 10, 2022

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

A non-powered, all- or partially-wheeled mobility aid in the form of a waist-high, foldable framework with handgrips 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 may also be used during rehabilitation. It is constructed of lightweight metal, plastic, and rubber materials and in the form of a mobile support structure which the patient holds and pushes in front of them as they walk. It is foldable for storage and transportation 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 TIPS AND PADS, CANE, CRUTCH AND WALKER devices

DRIVEMEDICAL RTL10365-ADJ
Drive Devilbiss Healthcare · TIPS AND PADS, CANE, CRUTCH AND WALKER
6 reports
DRIVEMEDICAL RTL10353
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 13, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
Page last rebuilt: Oct 13, 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