MyWay Walker Chassis - Product Usage: is intended for recall
MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
Why was MyWay Walker Chassis - Product Usage: is intended for recalled?
Due to a failure of the welds, the casters detached from the rear legs of the walker.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
- Recalling firm
- James Leckey Design Ltd
- Quantity
- 2,719 walkers
- 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.
- Recall date
- June 2, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)