Device recall
Z-2355-2024: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the…
FDA device recall · Class II · Medical Depot Inc.
Key facts
| Recall number (Z-number) | Z-2355-2024 |
|---|---|
| Recall event | 94832 |
| 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: 791RD (Red) |
| Product code | ITJ |
| Recalling firm | Medical Depot Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002997602 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database