There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send GE Healthcare Finland Oy to request your refund or repair — edit it as you like.
Subject: Recall Z-2033-2023 — GE Healthcare Finland Oy GE Healthcare Finland Oy recalls TruSignal Integrated Ear Sensor with Date Hello, I own a GE Healthcare Finland Oy recalls TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter that is covered by recall Z-2033-2023 from GE Healthcare Finland Oy. 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.
