FULL VISION INC — Class II medical device recall Z-0368-2023
Ongoing recall by Full Vision Inc, reported 2022-12-14, distributed in GA, NY. This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-u
| Recall number | Z-0368-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Full Vision Inc, Newton, KS, United States |
| Recall initiated | 2022-08-31 |
| Classified | 2022-12-02 |
| Reported by FDA | 2022-12-14 |
| Distributed | GA, NY |
| Countries outside the US | MX |
| Quantity | 69 units |
| Reason classes | device malfunction |
| UPC / GTIN / 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 and 44 more |
| Model numbers | 317-07926GE |
Product
FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0368-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.