Agency classClass IIOur severity:High FDA (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.

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: 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: sudden-stop
unexpected-reversal
unexpected-acceleration
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 →

Same manufacturer · Full Vision Inc

See all →

High
TrackMaster TMX428 Treadmill drive circuit board malfunction recall
FDA (Devices) · 2023-07-12
High
TrackMaster Treadmill Recalled for Drive PCB Malfunction Risk
FDA (Devices) · 2023-07-12
High
Treadmill recalled for drive PCB malfunction causing unexpected acceleration
FDA (Devices) · 2023-07-12
High
TrackMaster Treadmill Drive PCB Malfunction Causes Unexpected Stop, Reverse, and Acceleration
FDA (Devices) · 2023-07-12
High
Treadmill Recalled for Drive PCB Malfunction Causing Unexpected Belt Movement
FDA (Devices) · 2023-07-12

Same hazard · sudden stop