Data Foundry

Medical device recalls 2022

FULL VISION INC — Class II medical device recall Z-0364-2023

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-0364-2023
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
Quantity106 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00860176000606
Serial numbersFVDC-7585, FVDC-7586, FVDC-7587, FVDC-7588, FVDC-7589, FVDC-7590, FVDC-7591, FVDC-7592, FVDC-7593, FVDC-7594, FVDC-7595, FVDC-7596, FVDC-7597, FVDC-7598, FVDC-7599, FVDC-7600, FVDC-7601, FVDC-7602, FVDC-7603, FVDC-7604, FVDC-7605, FVDC-7606, FVDC-7607, FVDC-7608, FVDC-7609 and 81 more
Model numbers317-07926

Product

FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926

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-0364-2023. 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.