FDA Enforcement Class II Ongoing

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)

Recall: Z-2355-2024 · Reported July 24, 2024

Enforcement

Recall Number
Z-2355-2024
Event ID
94832
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Medical Depot Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
July 24, 2024
Initiation Date
June 14, 2024
Classification Date
July 12, 2024
Address
99 Seaview Blvd Fl 2, Port Washington, NY, 11050-4606, United States

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

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

Code Info

UPC: 822383019086 (791RD) All serial numbers beginning with 21S

Distribution

Nationwide Foreign: Canada

Quantity

667 units