GE Healthcare Finland recalls TruSignal Sensitive Skin Sensor REF TS-SE-3 oximeters due to potential defibrillation energy reduction and inaccurate measurements. Affected units sold in the US.
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
GE Healthcare Finland is recalling Tru:Signal Sensitive Skin Sensors with model REF TS-SE-3 because they might not deliver proper defibrillation energy or give inaccurate readings. This could affect medical safety during critical procedures.
The device may not deliver sufficient energy during defibrillation, which could be life-threatening for patients needing cardiac treatment. It might also provide inaccurate blood oxygen readings, leading to incorrect medical decisions.
Healthcare providers using the device for patient monitoring are most at risk. Patients receiving defibrillation treatments could be affected if the device is used incorrectly.
Check for the model number REF TS-SE-3 on the device. The product was sold in the US with GTIN 00840682103282.
Look for the model number REF TS-SE-3 on the device label.
The recall states there is a potential reduction in defibrillation energy or inaccurate measurements, which could affect patient safety during critical procedures.
Check for the model number REF TS-SE-3 on the device label. The product was sold in the US with GTIN 00840682103282.
The recall does not specify a remedy, so contact GE Healthcare Finland directly for guidance.
We’ve drafted a message you can send GE Healthcare Finland to request your refund or repair — edit it as you like.
Subject: Recall Z-2028-2023 — GE Healthcare Finland GE Healthcare Finland Hello, I own a GE Healthcare Finland that is covered by recall Z-2028-2023 from GE Healthcare Finland. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
