Full Vision Inc. Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class II: 7.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA recall — FDA Z-2058-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929 recall — FDA Z-2055-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926 recall — FDA Z-2052-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE recall — FDA Z-2057-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE recall — FDA Z-2056-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927 recall — FDA Z-2053-2023

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

Class IIFDA: OngoingFull Vision Inc.

Medical DeviceJul 12, 2023

Full Vision TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 recall — FDA Z-2054-2023

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

Class IIFDA: OngoingFull Vision Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Full Vision Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.