Device recall: FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926
FDA enforcement event 90995 is a device recall by Full Vision Inc of Newton, KS, initiated 31 Aug 2022 and classified Class II, with 7 product records.
FDA defines Class II as 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. 88% of the 839 device enforcement events initiated in 2022 carry the same class.
Status: Ongoing. Initiation: voluntary: firm initiated. Full Vision Inc has 2 enforcement events on this register, with a median of 7 product records per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Full Vision Inc, Newton, KS.
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."
Distribution
"Wi, GA, NY, Mexico"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0364-2023 | FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926 | 106 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0365-2023 | FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927 | 38 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0366-2023 | FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928 | 4 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0367-2023 | FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929 | 3 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0368-2023 | FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE | 69 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0369-2023 | FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE | 165 units | Class II | Ongoing | 14 Dec 2022 |
| Z-0370-2023 | FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE CHINA | 8 units | Class II | Ongoing | 14 Dec 2022 |
Context
Other enforcement events for Full Vision Inc
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 12 May 2023 | TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926 | Device | Class II | 7 |
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. 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.
Where was the product distributed?
FDA's distribution pattern field reads: "Wi, GA, NY, Mexico"
Is the recall still ongoing?
FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.