The Recall Desk
HighFDA (Devices)·Z-0366-2023·Announced 2022-12-14

Full Vision TrackMaster Treadmill Safety Tether May Fail During Fall

Full Vision Inc. is recalling TrackMaster treadmills due to a circuit defect in the safety tether. If the magnet detaches during a fall, the treadmill may fail to stop.

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 with no reported illnesses or injuries. The defect affects a safety-critical function (emergency stop), creating a risk-of-harm scenario. Per the rubric, with no reported harm and a theoretical injury risk, the score is High (3).

Plain-English summary

Full Vision Inc. is recalling 4 units of the TrackMaster treadmill (Model #317-07928, 110V). The affected serial numbers are FVDC-7644, FVDC-7645, FVDC-7646, and FVDC-7686. These units were distributed in Wisconsin, Georgia, New York, and Mexico.

The treadmill's Magnetic Safety Tether—an emergency stop mechanism—is controlled by a circuit that can enter a rare latch-up condition. When this occurs, pulling the magnet to activate the emergency stop during a fall may not work, and the treadmill may fail to stop.

This defect could leave a user on a moving treadmill if they fall. The hazard is rare and occurs only under specific conditions, but the potential consequence is serious.

If you own one of these treadmills, contact Full Vision Inc. for information on this recall.

The recalled product

Product
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928
Manufacturer
Full Vision Inc
Category
Medical Device — Exercise Equipment
Hazard
Affected units
4

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 (5)

  • UDI/DI 00860176000620
  • Serial Numbers: FVDC-7644
  • FVDC-7645
  • FVDC-7646
  • FVDC-7686

Distribution

Distributed in 3 states:

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 · emergency stop failure

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