Data Foundry

Medical device recalls 2023

TRACKMASTER — Class II medical device recall Z-2056-2023

Ongoing recall by Full Vision Inc, reported 2023-07-12, distributed nationwide. Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

Recall numberZ-2056-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmFull Vision Inc, Newton, KS, United States
Recall initiated2023-05-12
Classified2023-06-30
Reported by FDA2023-07-12
DistributedNationwide (US)
Countries outside the USAE, AU, BH, CA, CL, CO, CR, DO, FI, GB, GT, HK, ID, IL, IN, KR, MX, NI, NZ, PA, PE, PH, SA, SG, TH, UA, UY
Quantity264 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00860176000668
Serial numbersGEDC-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 239 more
Model numbers317-07926GE

Product

TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE

Reason for recall

Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

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-2056-2023. 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.