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Recall Observatory FDA recall evidence

Device 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: 791BL (Blue)

Z-2354-2024

June 14, 2024

Class II

Product summary

Firm
Medical Depot Inc.
Event
Event 94832
Status
Ongoing
Classification
Class II
Quantity
875 units
Official record key
device-enforcement:Z-2354-2024

Official wording

Reason: The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury

Code information: UPC: 822383019093 (791BL) All serial numbers beginning with 21S

Distribution pattern: Nationwide Foreign: Canada

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury