Medical device recalls Moderate risk

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

Recall date
August 31, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0369-2023
FDA classification
Class II
Brand / firm
Full Vision Inc
Sold / distributed
Wi, GA, NY, Mexico

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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