Recall Z-2355-2024— Medical Depot Inc.
Class II · Ongoing
Class II FDA medical device recall by Medical Depot Inc., initiated 2024-06-14. FDA's recall record names no specific 510(k) clearance for this event. 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: The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury.
- Recalling firm
- Medical Depot Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-06-14
- Firm location
- Port Washington, NY, United States
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.