Full Vision Trackmaster Treadmill Safety Tether May Fail During Falls
Eight Full Vision Trackmaster treadmills may fail to stop if the magnetic safety tether is pulled during a fall, due to a PCB circuit defect in the tether control system.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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 involving a PCB circuit defect that prevents the magnetic safety tether from functioning properly. The hazard is treadmill failure to stop during a fall—a serious injury risk. No illnesses or injuries have been reported; the hazard is theoretical under specific scenarios, meeting the criterion for a risk-of-harm product without yet-reported injury.
Plain-English summary
Full Vision Inc is recalling eight TRACKMASTER TREADMILL GE T2100-ST2 220V units (model 317-07927GE) with serial numbers GEDC-6765 through GEDC-6852.
The magnetic safety tether system has a defect in the PCB circuit that controls its safety function. Under specific scenarios, this circuit can enter a latch-up condition. When this occurs and the magnet is pulled loose—such as during a fall—the treadmill may fail to stop.
The affected units were distributed in Wisconsin, Georgia, New York, and Mexico.
The recalled product
- Product
- FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE CHINA
- Manufacturer
- Full Vision Inc
- Affected units
- 8
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 (9)
- UDI/DI 00860176000675
- Serial Numbers: GEDC-6765
- GEDC-6766
- GEDC-6767
- GEDC-6768
- GEDC-6849
- GEDC-6850
- GEDC-6851
- GEDC-6852
Distribution
Part of a larger recall action
This product is one of 7 recalled by Full Vision Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
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Same hazard · safety tether failure
See all →- HighTreadmill Magnetic Safety Tether May Fail to Stop During Fall
FDA (Devices) · 2022-12-14
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