Data Foundry

Medical device recalls 2022

FULL VISION INC — Class II medical device recall Z-0365-2023

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 numberZ-0365-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmFull Vision Inc, Newton, KS, United States
Recall initiated2022-08-31
Classified2022-12-02
Reported by FDA2022-12-14
DistributedGA, NY
Countries outside the USMX
Quantity38 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00860176000613
Serial numbersFVDC-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 and 13 more
Model numbers317-07927

Product

FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927

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-0365-2023. 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.