Data Foundry

Medical device recalls 2022

FULL VISION INC — Class II medical device recall Z-0369-2023

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-0369-2023
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
Quantity165 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00860176000675
Serial numbersGEDC-6608, GEDC-6609, GEDC-6610, GEDC-6611, GEDC-6612, GEDC-6613, GEDC-6614, GEDC-6615, GEDC-6616, GEDC-6617, GEDC-6618, GEDC-6619, GEDC-6620, GEDC-6621, GEDC-6622, GEDC-6623, GEDC-6624, GEDC-6625, GEDC-6626, GEDC-6627, GEDC-6628, GEDC-6629, GEDC-6630, GEDC-6631, GEDC-6682 and 140 more
Model numbers317-07927GE

Product

FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE

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-0369-2023. 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.