FDA Device recall Z-1687-2021
MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device
- FDA Device
- Class II
- ongoing
- Published 2021-06-02
On 2021-06-02 the FDA classified a Class II recall of MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device by James Leckey Design, citing due to a failure of the welds, the casters detached from the rear legs of the walker.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1687-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-01 |
| Published | 2021-06-02 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | James Leckey Design |
| Distribution | US |
Product
MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
Reason
Due to a failure of the welds, the casters detached from the rear legs of the walker.
Identifiers
| code_info | Catalog Codes/Item Number: S1 - 173-1600/PMWS1x; S2 - 173-2600/PMWS2x ; S3 - 173-3600/PMWS3x; Serial Number Range…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1687-2021%22
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