Class II
Medical Device Recall: 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)
Medical Depot Inc. · June 14, 2024
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
States Affected
NATIONWIDE
Quantity Affected
875 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2354-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.