RegWardenFDA facility compliance records
Recall

Class II — James Leckey Design Ltd

Recalling firmJames Leckey Design Ltd
Registered facilityFIREFLYFRIENDS LTD (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonDue to a failure of the welds, the casters detached from the rear legs of the walker.
ProductMyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
Quantity2,719 walkers
DistributionWorldwide 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 Fran…
Initiated2021-03-01
Classified2021-05-27
Recall numberZ-1687-2021
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — James Leckey Design Ltd (Z-1687-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87804/

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