The Recall Desk
HighFDA (Devices)·Z-2057-2023·Announced 2023-07-12

TrackMaster GE Treadmill Recall Due to Drive Circuit Board Malfunction

Full Vision Inc is recalling 1,416 TrackMaster GE T2100-ST2 220V treadmills worldwide due to a drive circuit board defect that can cause the treadmill to stop suddenly, reverse unexpectedly, or accelerate forward, posing a risk of falls or injury.

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 treadmill with a malfunction that can cause sudden stops, reversals, and unexpected acceleration, posing clear risk of falls or impact injuries. No illnesses or injuries have been reported, which per the severity rubric places this at the maximum score for theoretical risk-of-harm products.

Plain-English summary

Full Vision Inc is recalling the TrackMaster GE T2100-ST2 220V treadmill (model 317-07927GE) due to a malfunction in the drive circuit board (PCB). The defective PCB can misread electronic signals, causing the treadmill to stop suddenly, reverse unexpectedly, or accelerate forward without user input.

This malfunction poses a risk of injury from unexpected and uncontrolled treadmill movement. Approximately 1,416 units have been distributed in the United States and internationally.

Consumers who own an affected treadmill should stop using it immediately and contact Full Vision Inc for instructions on repair, replacement, or return. Check your treadmill's serial number against the official recall notice to confirm if your unit is affected.

The recalled product

Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE
Manufacturer
Full Vision Inc
Category
Medical Device — Exercise Equipment
Hazard
Affected units
1,416

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 00860176000675
  • Serial Numbers: GEDC-6608
  • GEDC-6609
  • GEDC-6610
  • GEDC-6611
  • GEDC-6612
  • GEDC-6613
  • GEDC-6614
  • GEDC-6615
  • GEDC-6616
  • GEDC-6617
  • GEDC-6618
  • GEDC-6619
  • GEDC-6620
  • GEDC-6621
  • GEDC-6622
  • GEDC-6623
  • GEDC-6624
  • GEDC-6625
  • GEDC-6626

Distribution

Distributed nationwide across the United 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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