---
title: "TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 — FDA record Z-2054-2023 | Is It on Recall"
description: "Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward."
url: https://isitonrecall.com/recall/fda-device-z-2054-2023-trackmaster-treadmill-tmx428cp-110v-model-number-317-07928/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 — FDA record Z-2054-2023

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 May 12, 2023. 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**: TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928
- **Reason**: Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
- **Classification**: Class II
- **Recalling firm**: Full Vision Inc
- **Quantity**: 39 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2054-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2054-2023%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 00860176000620, Serial Numbers: FVDC-7644, FVDC-7645, FVDC-7646, FVDC-7686, FVDC-7786, FVDC-7888, FVDC-7927, FVDC-8192, FVDC-8255, FVDC-8310, FVDC-8316, FVDC-8317, FVDC-8318, FVDC-8319, FVDC-8320, FVDC-8321, FVDC-8322, FVDC-8323, FVDC-8324, FVDC-8325, FVDC-8386, FVDC-8387, FVDC-8416, FVDC-8542, FVDC-8543, FVDC-8544, FVDC-8545, FVDC-8546, FVDC-8547, FVDC-8617, FVDC-8618, FVDC-8731, FVDC-8802, FVDC-8809, FVDC-8810, FVDC-8812, FVDC-8813, FVDC-8815, FVDC-8816 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

USA (Nationwide), Australia, Bahrain, Canada, Chile, Colombia, Costa Rica, Dominican Republic, FINLAND, Guatemala, HONG KONG, India, Indonesia, Israel, Mexico, NEW ZEALAND, Nicaragua, Panama, PARAQUAY, Peru, Philippines, Saudi Arabia, Singapore, SOUTH KOREA, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uruguay

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jul 12, 2023
- **Recall initiation date**: May 12, 2023
- **Center classification date**: Jun 30, 2023

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-2054-2023%22)

## Related records

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