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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