Class II — Medical Depot Inc.
| Recalling firm | Medical Depot, Inc DBA Drive DeVilbiss Healthcare |
|---|---|
| Registered facility | AmFab Co., LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury |
| 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) |
| Quantity | 875 units |
| Distribution | Nationwide Foreign: Canada |
| Initiated | 2024-06-14 |
| Classified | 2024-07-12 |
| Recall number | Z-2354-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medical Depot Inc. (Z-2354-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94832/
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