James Leckey Design Ltd recalls MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.

Recall date

March 1, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1687-2021

FDA classification

Class II

Brand / firm

James Leckey Design Ltd

Sold / distributed

Worldwide distribution - U.S. Nationwide distribution in the states of CA and WI and the countries of Italy, Norway, Australia, Czechia, Netherlands, Denmark, New Zealand, Japan, United Arab Emirates, Qatar, Croatia, Spain, Poland, Russia, South Africa, Taiwan, Saudi Arabia, Chemitec, Centre Harika…

Why it was recalled

Due to a failure of the welds, the casters detached from the rear legs of the walker.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.