Treadmill Safety Tether Circuit Defect May Prevent Emergency Stop
Full Vision Inc. Trackmaster treadmills have a rare circuit defect that may prevent the safety tether from stopping the machine during a fall.
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: FDA Class II recall of a safety mechanism (Magnetic Safety Tether) that may fail to activate during an emergency. The hazard is concrete and real—a circuit defect under specific conditions. No injuries or deaths have been reported, but the potential for serious injury exists if the emergency stop fails during a fall.
Plain-English summary
Full Vision Inc. is recalling three Trackmaster treadmills (Model #317-07929, 220V) due to a rare defect in the safety mechanism.
The affected treadmills contain a circuit defect on the control board that manages the Magnetic Safety Tether. Under specific conditions, the circuit can enter a latch-up state. If a user falls and pulls the magnetic tether to trigger the emergency stop, the circuit may fail to respond and the treadmill may continue running instead of stopping.
Three units with serial numbers FVDC-7641, FVDC-7642, and FVDC-7643 were distributed to Wisconsin, Georgia, New York, and Mexico.
If you own an affected treadmill, discontinue use immediately. Contact Full Vision Inc. for repair or replacement instructions. Do not operate the machine until the safety circuit has been inspected or corrected.
The recalled product
- Product
- FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929
- Manufacturer
- Full Vision Inc
- Hazard
- safety-mechanism-failure
- fall-injury-risk
- circuit-defect
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 (4)
- UDI/DI 00860176000637
- Serial Numbers: FVDC-7641
- FVDC-7642
- FVDC-7643
Distribution
Distributed in 2 states:
- GA
- NY
Related recalls
Same category
- SevereDa Vinci surgical system operative components with E-brake retainer pin defect
FDA (Devices) · 2026-07-01
- SevereMedline angiography and radiology convenience kits recalled for unapproved design changes
FDA (Devices) · 2026-07-01
- ModerateOctopus Evolution AS Tissue Stabilizer Model TS2500 Tubing Assembly Issue Recall
FDA (Devices) · 2026-07-01
- ModerateOctopus 4 Tissue Stabilizer incorrectly assembled tubing positions
FDA (Devices) · 2026-07-01
- SevereMedical Device Surgical Kits with Syringes Recalled for Unapproved Design Changes
FDA (Devices) · 2026-07-01