The Recall Desk
HighFDA (Devices)·Z-0368-2023·Announced 2022-12-14

Treadmill safety mechanism may fail to stop during fall

Full Vision Inc. Trackmaster treadmills (Model #317-07926GE) may fail to stop during a fall if the magnetic safety mechanism malfunctions. 69 units are affected.

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 a Class II FDA recall for failure of a critical safety mechanism designed to stop the treadmill during falls. No injuries have been reported, but the hazard presents a direct risk of injury; per the rubric, risk-of-harm products without reported harm are scored as High (3).

Plain-English summary

Full Vision Inc. has recalled the Trackmaster treadmill (Model #317-07926GE, 110V) due to a potential failure of the magnetic safety tether. This safety mechanism is designed to stop the treadmill if the user falls.

Under specific conditions, the circuit controlling the magnetic safety tether can enter a latch-up condition. If this occurs and the magnet is pulled loose during a fall, the treadmill may not stop.

The recall affects 69 units distributed in Wisconsin, Georgia, New York, and Mexico. Affected units have serial numbers ranging from GEDC-6632 through GEDC-6847. Consumers with affected treadmills can reference FDA recall number Z-0368-2023 for additional information.

The recalled product

Product
FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE
Manufacturer
Full Vision Inc
Category
Medical Device — Exercise Equipment
Hazard
Affected units
69

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 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 →

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