FDA recall Z-2355-2024

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: 791RD (Red)

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

Key facts

Status

Ongoing

Initiation date

2024-06-14

Report date

2024-07-24

Voluntary/Mandated

Voluntary: Firm initiated

Location

Port Washington, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2355-2024