Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remai...
FDA Recall #Z-2354-2024 — Class II — June 14, 2024
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: 791BL (Blue)
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
Recalling Firm
Medical Depot Inc. — Port Washington, NY
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
875 units
Distribution
Nationwide Foreign: Canada
Code Information
UPC: 822383019093 (791BL) All serial numbers beginning with 21S
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated