FULL VISION, INC.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
Devices registered here (1)
- Treadmill, PoweredProduct code IOL (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5380
Recalls & enforcement
- Class IIOngoing2023-05-12Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
- Class IIOngoing2022-08-31This 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 s…
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “FULL VISION, INC. (FEI 3001040337) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3001040337-full-vision-inc/
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