FDA Device recall Z-2056-2023
TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE
- FDA Device
- Class II
- ongoing
- Published 2023-07-12
On 2023-07-12 the FDA classified a Class II recall of TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE by Full Vision, citing treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2056-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-12 |
| Published | 2023-07-12 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Full Vision |
| Distribution | US |
Product
TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE
Reason
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
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, GEDC-6848, GEDC-7012, GEDC-7013, GEDC-7014, GEDC-7015, GEDC-7016, GEDC-7017, GEDC-7018, GEDC-7019, GEDC-7020, GEDC-7021, GEDC-7022, GEDC-7023, GEDC-7064, GEDC-7065, GEDC-7066, GEDC-7067, GEDC-7068, GED |
|---|
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-2056-2023%22
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