Recall Z-2053-2023— Full Vision Inc

Class II · Ongoing

Class II FDA medical device recall by Full Vision Inc, initiated 2023-05-12. FDA's recall record names no specific 510(k) clearance for this event. Product: TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927. Reason: Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward..

Recalling firm
Full Vision Inc
Classification
Class II
Status
Ongoing
Initiated
2023-05-12
Firm location
Newton, KS, United States

Product description

TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.