MyWay Walker Chassis — Class II medical device recall Z-1687-2021
Ongoing recall by James Leckey Design Ltd, reported 2021-06-02, distributed nationwide. Due to a failure of the welds, the casters detached from the rear legs of the walker.
| Recall number | Z-1687-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | James Leckey Design Ltd, Lisburn, N/A, United Kingdom |
| Recall initiated | 2021-03-01 |
| Classified | 2021-05-27 |
| Reported by FDA | 2021-06-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BE, CN, CZ, DK, ES, FR, HK, HR, ID, IT, JP, LB, MY, NL, NO, NZ, PH, PL, QA, RU, SA, SG, SK, TW, ZA |
| Quantity | 2,719 walkers |
| Reason classes | device malfunction |
| Model numbers | 173-1600/PMWS1X |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1687-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.