Nitro Glide Knee Walker-offers users recovering from a below-the-knee… — Class II medical device recall Z-2354-2024
Ongoing recall by Medical Depot Inc., reported 2024-07-24, distributed nationwide. The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustai
| Recall number | Z-2354-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Depot Inc., Port Washington, NY, United States |
| Recall initiated | 2024-06-14 |
| Classified | 2024-07-12 |
| Reported by FDA | 2024-07-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 875 units |
| UPC / GTIN / UDI-DI | 00822383019093 |
| Model numbers | 791BL |
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 for recall
The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2354-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.