James Leckey Design Ltd: Medical Device Recall in 2021 - (Recall #: Z-1687-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 1, 2021

Date Posted: June 2, 2021

Recall Number: Z-1687-2021

Event ID: 87804

Reason for Recall:

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

Status: Ongoing

Product Quantity: 2,719 walkers

Code Information:

Catalog Codes/Item Number: S1 - 173-1600/PMWS1x; S2 - 173-2600/PMWS2x ; S3 - 173-3600/PMWS3x; Serial Number Range: 220568 to 272111 manufactured between 08/01/2018 to 11/26/2020

Distribution Pattern:

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, Hong Kong, Lebanon, Belgium, Philippines, Singapore, Malaysia, Indonesia, Slovakia, China, and France.

Voluntary or Mandated:

Voluntary: Firm initiated