James Leckey MyWay Walker Chassis Recalled Due to Weld Failure
James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a structural defect in a medical device intended for children, posing a risk of harm through falling or instability, but the source text does not report any specific injuries or illnesses.
Plain-English summary
James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units. These devices are intended for use by children who are already using a supportive walking device. The recall is due to a failure of the welds, which caused the casters to detach from the rear legs of the walker.
The affected units have catalog codes S1 (173-1600/PMWS1x), S2 (173-2600/PMWS2x), and S3 (173-3600/PMWS3x). The serial numbers range from 220568 to 272111, and the units were manufactured between August 1, 2018, and November 26, 2020.
The product was distributed worldwide, including in the United States (California and Wisconsin) and numerous international locations such as Italy, Norway, Australia, and Japan. Consumers should stop using the affected walkers immediately and contact the manufacturer for instructions on repair or replacement.
The recalled product
- Product
- MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
- Manufacturer
- James Leckey Design Ltd
- Category
- Medical Device — Mobility Aids
- Affected units
- 2,719
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Catalog Codes/Item Number: S1 - 173-1600/PMWS1x
- S2 - 173-2600/PMWS2x
- S3 - 173-3600/PMWS3x
Distribution
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