Recall archive / FDA device enforcement
FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926 — FDA record Z-0364-2023
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 31, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926
- 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.
- Classification
- Class II
- Recalling firm
- Full Vision Inc
- Quantity
- 106 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0364-2023
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 00860176000606, Serial Numbers: FVDC-7585, FVDC-7586, FVDC-7587, FVDC-7588, FVDC-7589, FVDC-7590, FVDC-7591, FVDC-7592, FVDC-7593, FVDC-7594, FVDC-7595, FVDC-7596, FVDC-7597, FVDC-7598, FVDC-7599, FVDC-7600, FVDC-7601, FVDC-7602, FVDC-7603, FVDC-7604, FVDC-7605, FVDC-7606, FVDC-7607, FVDC-7608, FVDC-7609, FVDC-7610, FVDC-7611, FVDC-7612, FVDC-7613, FVDC-7614, FVDC-7615, FVDC-7616, FVDC-7617, FVDC-7618, FVDC-7619, FVDC-7620, FVDC-7621, FVDC-7622, FVDC-7623, FVDC-7624, FVDC-7625, FVDC-7626, FVDC-7627, FVDC-7628, FVDC-7629, FVDC-7640, FVDC-7666, FVDC-7667, FVDC-7668, FVDC-7669, FVDC-7670, FVDC-7671, FVDC-7672, FVDC-7673, FVDC-7674, FVDC-7675, FVDC-7676, FVDC-7677, FVDC-7678, FVDC-7679, FVDC-7680, FVDC-7681, FVDC-7682, FVDC-7683, FVDC-7684, FVDC-7685, FVDC-7687, FVDC-7688, FVDC-7689, FVDC-7690, FVDC-7691, FVDC-7692, FVDC-7693, FVDC-7694, FVDC-7695, FVDC-7696, FVDC-7697, FVDC-7698, FVDC-7699, FVDC-7700, FVDC-7701, FVDC-7702, FVDC-7703, FVDC-7704, FVDC-7705, FVDC-7706, FVDC-7717, FVDC-7719, FVDC-7720, FVDC-7721, FVDC-7722, FVDC-7723, FVDC-7724, FVDC-7725, FVDC-7726, FVDC-7727, FVDC-7728, FVDC-7729, FVDC-7730, FVDC-7731, FVDC-7732, FVDC-7733, FVDC-7734, FVDC-7735, FVDC-7736, FVDC-7737 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Wi, GA, NY, Mexico
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Dec 14, 2022
- Recall initiation date
- Aug 31, 2022
- Center classification date
- Dec 2, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.