Trackmaster TMX428CP 110VRecalls & reported problems
Full Vision, Inc. · TMX428CP 110V Trackmaster Treadmill · Class 1
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 12, 2023Open, Classified
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Z-2054-2023 · Root cause: Other · FDA record ↗
- Aug 31, 2022Open, Classified
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.
Z-0366-2023 · Root cause: Other · FDA record ↗
Other Treadmill, Powered devices
- T2100-ST T2100-ST2Full Vision, Inc. · Treadmill, Powered4 recalls0 reports
- T2100-ST T2100-ST1Full Vision, Inc. · Treadmill, Powered2 recalls0 reports
- Trackmaster TMX428 110VFull Vision, Inc. · Treadmill, Powered2 recalls0 reports
- Trackmaster TMX428CP 220VFull Vision, Inc. · Treadmill, Powered2 recalls0 reports
- Trackmaster TMX428 220VFull Vision, Inc. · Treadmill, Powered2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.