FDA Device recall 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 act…
- FDA Device
- Class II
- ongoing
- Published 2024-07-24
On 2024-07-24 the FDA classified a Class II recall of Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily act… by Medical Depot, citing the tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2354-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-14 |
| Published | 2024-07-24 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medical Depot |
| Distribution | US |
Product
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
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Identifiers
| upc | 822383019093 |
|---|---|
| code_info | UPC: 822383019093 (791BL) All serial numbers beginning with 21S |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2024%22
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