Facility

FULL VISION, INC.

2 recall(s) on record — most severe on record: Class II.

Key facts

2recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3001040337
Establishment type	Manufacture Medical Device
Location	3017 FULL VISION DR. NEWTON, KS, US 67114
Registration status	Active · expires 2026
Parent company	FULL VISION, INC. (owner-operator 9049599)
Brand names	TRACKMASTER TREADMILLS

Activity by year

Recalls (2)

Devices registered here (1)

Treadmill, Powered
Product code IOL (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5380

Recalls & enforcement

Class IIOngoing2023-05-12
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Class IIOngoing2022-08-31
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 s…

All facilities operated by FULL VISION, INC.

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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