Medical Depot Inc.: Medical Device Recall in 2024 - (Recall #: Z-2355-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

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: 791RD (Red)

Product Classification:

Class II

Date Initiated: June 14, 2024

Date Posted: July 24, 2024

Recall Number: Z-2355-2024

Event ID: 94832

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

Status: Ongoing

Product Quantity: 667 units

Code Information:

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

Distribution Pattern:

Nationwide Foreign: Canada

Voluntary or Mandated:

Voluntary: Firm initiated