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: 791RD (Red)

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

667 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2355-2024

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.

Medical Depot Inc. 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: 791RD (Red) | SafeCheck