CLASS II ONGOING Device recall · Reported 14 Dec 2022 · FDA Enforcement Report
Trackmaster, Treadmill Ge T2100-st2 220v recalled by Full Vision
Full Vision is recalling Full Vision Inc. Trackmaster, Treadmill Ge T2100-st2 220v, distributed in Georgia, New York. The recall was initiated on 31 Aug 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0370-2023
- FDA event ID
- 90995
- Recalling firm
- Full Vision, Newton, KS
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 31 Aug 2022
- FDA classified
- 2 Dec 2022
- Reported
- 14 Dec 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 31 Aug 2022 | Recall initiated by company | |
| 2 Dec 2022 | Classified by FDA | +93 days |
| 14 Dec 2022 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet is pulled loose as during a fall, the treadmill may fail to stop.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE CHINA
Where it was distributed
Wi, GA, NY, Mexico
Questions about this recall
Is Trackmaster, Treadmill Ge T2100-st2 220v recalled?
Yes. Full Vision recalled Trackmaster, Treadmill Ge T2100-st2 220v on 31 Aug 2022. The recall is Class II and its status is Ongoing. Recall number Z-0370-2023.
Why was it recalled?
This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet is pulled loose as during a fall, the treadmill may fail to stop.
Which lots are affected?
UDI/DI 00860176000675, Serial Numbers: GEDC-6765, GEDC-6766, GEDC-6767, GEDC-6768, GEDC-6849, GEDC-6850, GEDC-6851, GEDC-6852
Where was it sold?
Wi, GA, NY, Mexico
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Full Vision
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|---|---|---|---|---|---|
| Device | CLASS II | Trackmaster, Treadmill Tmx428cp 110v recalled by Full Vision | Full Vision | Device Malfunction | Nationwide |
| Device | CLASS II | Trackmaster, Treadmill Tmx428 220v recalled by Full Vision | Full Vision | Device Malfunction | Nationwide |
| Device | CLASS II | Trackmaster, Treadmill Ge T2100-st1 110vv recalled by Full Vision | Full Vision | Device Malfunction | Nationwide |
| Device | CLASS II | Trackmaster, Treadmill Ge T2100-st2 220v recalled by Full Vision | Full Vision | Device Malfunction | Nationwide |
| Device | CLASS II | Trackmaster, Treadmill Tmx428 110v recalled by Full Vision | Full Vision | Device Malfunction | Nationwide |
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