# FDA recall Z-2355-2024

> **Medical Depot Inc.** · Class II · device recall initiated 2024-06-14.

## 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)

## 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

## Distribution

Nationwide Foreign: Canada

## Key facts

- **Recall number:** Z-2355-2024
- **Recalling firm:** Medical Depot Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-14
- **Report date:** 2024-07-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Port Washington, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2355-2024

## Citation

> AI Analytics. FDA recall Z-2355-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2355-2024. Source: US FDA. Licensed CC0.

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