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Recall

Class II — Full Vision Inc

Recalling firmFULL VISION, INC.
Registered facilityFULL VISION, INC. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonTreadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
ProductTRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926
Quantity565 units
DistributionUSA (Nationwide), Australia, Bahrain, Canada, Chile, Colombia, Costa Rica, Dominican Republic, FINLAND, Guatemala, HONG KONG, India, Indonesia, Israel, Mexico, NEW ZEALAND, Nicaragua, Panama, PARAQUAY, Peru, Philippines, Saudi Arabia, Singapore, SOUTH KOREA, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uruguay
Initiated2023-05-12
Classified2023-06-30
Recall numberZ-2052-2023
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 — Full Vision Inc (Z-2052-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92382/

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