TrackMaster Treadmill Control Malfunction Can Cause Unexpected Acceleration
Full Vision's TrackMaster treadmill can experience drive PCB malfunctions causing unexpected stopping, reversal, and acceleration. The malfunction affects 264 units distributed worldwide.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall of exercise equipment with a documented control system malfunction that poses a risk of injury, but no illnesses or injuries have been reported in the source text. Per the rubric, this qualifies as a risk-of-harm product where injury has not yet been reported, placing it at severity level 3 (High).
Plain-English summary
Full Vision Inc. is recalling the TrackMaster Treadmill GE T2100-ST1, model 317-07926GE, due to a malfunction in the drive printed circuit board. The PCB can misread signals, causing the treadmill to stop, reverse, and then accelerate forward unexpectedly.
This recall affects 264 units with serial numbers ranging from GEDC-6632 to GEDC-8347. The affected treadmills have been distributed to customers in the United States and internationally, including Australia, Canada, India, Mexico, the Philippines, the United Kingdom, and other countries.
The control system malfunction poses a risk when the treadmill unexpectedly stops, reverses, or accelerates. Users may lose balance or be struck by the equipment during these malfunctions.
Consumers with affected TrackMaster treadmills should stop using the equipment and contact Full Vision Inc. for repair or replacement instructions. For additional information, consumers can reference FDA recall number Z-2056-2023.
The recalled product
- Product
- TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE
- Manufacturer
- Full Vision Inc
- Hazard
- sudden-stop
- unexpected-reversal
- unexpected-acceleration
- control-failure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- UDI/DI 00860176000668
- Serial Numbers: GEDC-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
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereMedtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
FDA (Devices) · 2026-05-27
- HighAzurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
FDA (Devices) · 2026-05-27
- HighSwan-Ganz Jr Catheter models recalled due to lumen hub leakage
FDA (Devices) · 2026-05-27
- SevereMedtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall
FDA (Devices) · 2026-05-27