FDA Device recall Z-0367-2023
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929
- FDA Device
- Class II
- ongoing
- Published 2022-12-14
On 2022-12-14 the FDA classified a Class II recall of FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929 by Full Vision, citing 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 Magne….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0367-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-08-31 |
| Published | 2022-12-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Full Vision |
| Distribution | GA, NY |
Product
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929
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.
Identifiers
| code_info | UDI/DI 00860176000637, Serial Numbers: FVDC-7641, FVDC-7642, FVDC-7643 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0367-2023%22
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