# FDA recall Z-1687-2021

> **James Leckey Design Ltd** · Class II · device recall initiated 2021-03-01.

## Product

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

## Reason for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-1687-2021
- **Recalling firm:** James Leckey Design Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-01
- **Report date:** 2021-06-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lisburn, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1687-2021

## Citation

> AI Analytics. FDA recall Z-1687-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1687-2021. Source: US FDA. Licensed CC0.

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