Recall Z-2057-2023— 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 GE T2100-ST2 220V, MODEL NUMBER 317-07927GE. 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 GE T2100-ST2 220V, MODEL NUMBER 317-07927GE
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.