FDA Device recall Z-2053-2023
TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927
- FDA Device
- Class II
- ongoing
- Published 2023-07-12
On 2023-07-12 the FDA classified a Class II recall of TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927 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-2053-2023 |
| 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 TMX428 220V, MODEL NUMBER 317-07927
Reason
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Identifiers
| code_info | UDI/DI 00860176000613, Serial Numbers: FVDC-7630, FVDC-7631, FVDC-7633, FVDC-7634, FVDC-7635, FVDC-7636, FVDC-7637, FV…UDI/DI 00860176000613, Serial Numbers: FVDC-7630, FVDC-7631, FVDC-7633, FVDC-7634, FVDC-7635, FVDC-7636, FVDC-7637, FVDC-7638, FVDC-7639, FVDC-7647, FVDC-7648, FVDC-7649, FVDC-7650, FVDC-7651, FVDC-7652, FVDC-7653, FVDC-7654, FVDC-7655, FVDC-7656, FVDC-7657, FVDC-7658, FVDC-7659, FVDC-7660, FVDC-7661, FVDC-7662, FVDC-7663, FVDC-7664, FVDC-7665, FVDC-7707, FVDC-7708, FVDC-7709, FVDC-7710, FVDC-7711, FVDC-7712, FVDC-7713, FVDC-7714, FVDC-7715, FVDC-7716, FVDC-7749, FVDC-7750, FVDC-7751, FVDC-7752, FVDC-7753, FVDC-7754, FVDC-7755, FVDC-7756, FVDC-7757, FVDC-7758, FVDC-7759, FVDC-7760, FVDC-7761, FVDC-7762, FVDC-7763, FVDC-7764, FVDC-7765, FVDC-7766, FVDC-7767, FVDC-7768, FVDC-7769, FVDC-7770, FVDC-7771, FVDC-7772, FVDC-7773, FVDC-7774, FVDC-7775, FVDC-7776, FVDC-7777, FVDC-7778, FVDC-7779, FVDC-7780, FVDC-7784, FVDC-7801, FVDC-7802, FVDC-7803, FVDC-7804, FVDC-7805, FVDC-7806, FVDC-7807, FVDC-7808, FVDC-7809, FVDC-7810, FVDC-7826, FVDC-7827, FVDC-7828, FVDC-7829, FVDC-7830, FVDC-7831, FVD |
|---|
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-2053-2023%22
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