RecallRadar

FDA Device recall Z-0368-2023

FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE

On 2022-12-14 the FDA classified a Class II recall of FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE 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

AgencyFDA Device
Recall numberZ-0368-2023
ClassificationClass II
Statusongoing
Initiated2022-08-31
Published2022-12-14
Last updated2026-09-13 11:56 UTC
CompanyFull Vision
DistributionGA, NY

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.

Identifiers

code_info
UDI/DI 00860176000668, Serial Numbers: GEDC-6632, GEDC-6633, GEDC-6634, GEDC-6635, GEDC-6636, GEDC-6637, GEDC-6638, GE…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

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-0368-2023%22

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