Class II — Full Vision Inc
| Recalling firm | FULL VISION, INC. |
|---|---|
| Registered facility | FULL VISION, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet is pulled loose as during a fall, the treadmill may fail to stop. |
| Product | FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929 |
| Quantity | 3 units |
| Distribution | Wi, GA, NY, Mexico |
| Initiated | 2022-08-31 |
| Classified | 2022-12-02 |
| Recall number | Z-0367-2023 |
| Initiation | Voluntary: 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-0367-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90995/
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