The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-2058-2023·Announced 2023-07-12

Treadmill recalled for drive PCB malfunction causing unexpected acceleration

Full Vision Inc recalls 95 TRACKMASTER GE T2100-ST2 treadmills with a defective drive PCB that may misread signals, causing the equipment to unexpectedly stop, reverse, or accelerate forward.

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 medical device recall involving a documented malfunction that presents risk of injury through unexpected acceleration, reversal, or stopping during use. No illnesses or injuries are reported in the source text. Per the rubric, risk-of-harm products where injury has not yet been reported are classified as High (Score 3).

Plain-English summary

Full Vision Inc is recalling 95 TRACKMASTER GE T2100-ST2 treadmills (220V model) due to a defect in the drive PCB. The PCB can misread operating signals, which may cause the treadmill to unexpectedly stop, reverse, or accelerate forward during use.

The affected units were distributed nationwide in the USA and internationally to 24 countries including Canada, United Kingdom, Mexico, Australia, Chile, Colombia, India, Indonesia, Israel, Japan, New Zealand, Philippines, Saudi Arabia, Singapore, South Korea, Thailand, and others. Affected units can be identified by model number 317-07927GE, UDI/DI code 00860176000675, and specific serial numbers beginning with GEDC (GEDC-6765 through GEDC-8018, as listed in FDA recall Z-2058-2023).

Consumers who own affected treadmills should stop using them immediately and contact Full Vision Inc for repair or replacement instructions. The FDA has assigned this recall number Z-2058-2023. A complete list of affected serial numbers is available through the FDA's official recall database.

The recalled product

Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
Manufacturer
Full Vision Inc
Category
Medical Device — Treadmill / Exercise Equipment
Hazard
Affected units
95

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-6765
  • GEDC-6766
  • GEDC-6767
  • GEDC-6768
  • GEDC-6849
  • GEDC-6850
  • GEDC-6851
  • GEDC-6852
  • GEDC-6995
  • GEDC-6996
  • GEDC-6997
  • GEDC-6998
  • GEDC-6999
  • GEDC-7000
  • GEDC-7001
  • GEDC-7002
  • GEDC-7003
  • GEDC-7004
  • GEDC-7005

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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