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TrackmasterRecalls & reported problems across all models

Full Vision, Inc. · 4 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

8 open recalls name at least one Trackmaster model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
8

We found 4 models of Trackmaster by Full Vision, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

8 FDA recall records name at least one of these models by its device identifier, 8 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Trackmaster recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. May 12, 2023Open, Classified

    Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

    Z-2055-2023 · Root cause: Other · Recall details · FDA record ↗

  2. 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 · Recall details · FDA record ↗

  3. May 12, 2023Open, Classified

    Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

    Z-2053-2023 · Root cause: Other · Recall details · FDA record ↗

  4. May 12, 2023Open, Classified

    Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

    Z-2052-2023 · Root cause: Other · Recall details · FDA record ↗

  5. 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-0367-2023 · Root cause: Other · Recall details · FDA record ↗

  6. 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 · Recall details · FDA record ↗

  7. 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-0365-2023 · Root cause: Other · Recall details · FDA record ↗

  8. 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-0364-2023 · Root cause: Other · Recall details · FDA record ↗

Trackmaster models

4 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Full Vision, Inc. products

All Full Vision, Inc. devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page