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FDAFDA · Food and drugs·Recall number Z-2354-2024

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: 791BL (Blue)

Published July 24, 2024 · Recall initiated: June 14, 2024

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
Medical Depot Inc.
Distributor
Nationwide Foreign: Canada
Lot
UPC: 822383019093 (791BL) All serial numbers beginning with 21S
Risk classification
Class II
Area (FDA)
device
Country
United States

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