Recall Z-1687-2021— James Leckey Design Ltd
Class II · Ongoing
Class II FDA medical device recall by James Leckey Design Ltd, initiated 2021-03-01. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- James Leckey Design Ltd
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2021-03-01
- Firm location
- Lisburn, N/A, United Kingdom
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.