---
title: "FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE — FDA record Z-0368-2023 | Is It on Recall"
description: "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 fu"
url: https://isitonrecall.com/recall/fda-device-z-0368-2023-full-vision-inc-trackmaster-treadmill-ge-t2100-st1-110v-model-317-07926ge/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE — FDA record Z-0368-2023

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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE
- **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**: 69 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0368-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0368-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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 00860176000668, Serial Numbers: GEDC-6632, GEDC-6633, GEDC-6634, GEDC-6635, GEDC-6636, GEDC-6637, GEDC-6638, GEDC-6639, GEDC-6640, GEDC-6641, GEDC-6642, GEDC-6643, GEDC-6644, GEDC-6645, GEDC-6646, GEDC-6647, GEDC-6648, GEDC-6649, GEDC-6650, GEDC-6651, GEDC-6652, GEDC-6653, GEDC-6654, GEDC-6655, GEDC-6656, GEDC-6657, GEDC-6658, GEDC-6659, GEDC-6660, GEDC-6661, GEDC-6662, GEDC-6663, GEDC-6664, GEDC-6665, GEDC-6666, GEDC-6667, GEDC-6668, GEDC-6669, GEDC-6670, GEDC-6671, GEDC-6672, GEDC-6673, GEDC-6674, GEDC-6675, GEDC-6676, GEDC-6677, GEDC-6678, GEDC-6679, GEDC-6680, GEDC-6681, GEDC-6755, GEDC-6756, GEDC-6757, GEDC-6758, GEDC-6759, GEDC-6760, GEDC-6761, GEDC-6762, GEDC-6763, GEDC-6764, GEDC-6839, GEDC-6840, GEDC-6841, GEDC-6842, GEDC-6843, GEDC-6844, GEDC-6845, GEDC-6846, GEDC-6847 |

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.

- [Georgia](https://isitonrecall.com/state/georgia/)
- [New York](https://isitonrecall.com/state/new-york/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0368-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Full Vision Inc records](https://isitonrecall.com/brand/full-vision-inc/)