GE Healthcare Finland recalls TruSignal Wrap Sensor (REF TS-W-D) due to potential reduction in defibrillation energy reaching patients. Affected units may cause inaccurate measurements or unintended electrical contact.
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 Wrap Sensors (REF TS-W-D) because they might not deliver proper defibrillation energy during emergencies, leading to inaccurate readings or electrical risks. This could affect patient safety during critical medical procedures.
The sensor could reduce the energy delivered during defibrillation, potentially failing to shock the heart properly in emergencies. It might also cause unintended electrical contact or provide inaccurate blood oxygen measurements.
Healthcare professionals using the TruSignal Wrap Sensor for defibrillation or oximetry are most at risk. Patients receiving care with this device may also be affected.
Check for the model reference 'TS-W-D' on the TruSignal Wrap Sensor. The product was sold with GTIN 00840682103121. This recall applies to GE Healthcare Finland's oximeter devices.
Look for the model reference 'TS-W-D' on the TruSignal Wrap Sensor.
Reach out to GE Healthcare Finland for specific guidance on next steps.
The recall states there is a potential reduction in defibrillation energy reaching patients, which could lead to inaccurate measurements or unintended electrical contact. This may affect patient safety during critical medical procedures.
Check for the model reference 'TS-W-D' on the TruSignal Wrap Sensor. The product was sold with GTIN 00840682103121.
The recall does not specify a remedy, so contact GE Healthcare Finland for specific 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-2029-2023 — GE Healthcare Finland GE Healthcare Finland Hello, I own a GE Healthcare Finland that is covered by recall Z-2029-2023 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.
