Medical Depot Inc.: Device Recall

Recall #Z-2355-2024 · 06/14/2024

Class II: Risk

Recall Details

Recall Number: Z-2355-2024
Classification: Class II
Product Type: Device
Recalling Firm: Medical Depot Inc.
Status: Ongoing
Date Initiated: 06/14/2024
Location: Port Washington, NY, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 667 units

Reason for Recall

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

Product Description

Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791RD (Red)

Distribution Pattern

Nationwide Foreign: Canada

Other Recalls by Medical Depot Inc.

Class I: Dangerous 04/11/2025

Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Class II: Risk 06/14/2024

The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

View all recalls by Medical Depot Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.