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TruSignal SpO2Recalls & reported problems across all models

GE Healthcare Finland Oy · 9 models in the FDA device registry

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

9 open recalls name at least one TruSignal SpO2 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
9

We found 9 models of TruSignal SpO2 by GE Healthcare Finland Oy in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

9 FDA recall records name at least one of these models by its device identifier, 9 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

TruSignal SpO2 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 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2034-2023 · Root cause: Device Design · Recall details · FDA record ↗

  2. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2033-2023 · Root cause: Device Design · Recall details · FDA record ↗

  3. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2032-2023 · Root cause: Device Design · Recall details · FDA record ↗

  4. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2031-2023 · Root cause: Device Design · Recall details · FDA record ↗

  5. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2030-2023 · Root cause: Device Design · Recall details · FDA record ↗

  6. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2029-2023 · Root cause: Device Design · Recall details · FDA record ↗

  7. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2028-2023 · Root cause: Device Design · Recall details · FDA record ↗

  8. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2027-2023 · Root cause: Device Design · Recall details · FDA record ↗

  9. May 19, 2023Open, Classified

    There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

    Z-2026-2023 · Root cause: Device Design · Recall details · FDA record ↗

TruSignal SpO2 models

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

Other GE Healthcare Finland Oy products

All GE Healthcare Finland Oy devices →

Sources and updates

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