Z-2354-2024 Class II Ongoing
FDA device recall Z-2354-2024 was initiated by Medical Depot Inc. on June 14, 2024 and is designated Class II. 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 The recall status is ongoing. Affected quantity: 875 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 24, 2024
- Initiation Date
- June 14, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 875 units
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: 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
Distribution Pattern
Nationwide Foreign: Canada
Code Information
UPC: 822383019093 (791BL) All serial numbers beginning with 21S