Philips recalls PageWriter TC30 cardiograph devices with specific software versions due to risk of overheating, melting, and fire. Affected units may cause injury to patients or users. Contact Philips for details.
Philips PageWriter TC cardiograph batteries which have reached end of life may overheat, causing the case to melt and/or the device to ignite, which can cause injury to patient or nearby users.
Philips is recalling PageWriter TC30 cardiograph devices with certain software versions because batteries may overheat, melt the device, or cause fire. This poses a risk of injury to patients or nearby users.
The batteries in these devices may reach end of life and overheat, causing the device casing to melt and potentially ignite. This fire hazard could injure patients or people in close proximity to the device.
Healthcare professionals using the PageWriter TC30 cardiograph device for patient evaluations are most at risk. Patients and others nearby could also be injured if the device ignites.
Check for the PageWriter TC30 with trolley Government Bundle, Product 860354, and software revisions up to A.07.05.22. The device is used for evaluating electrocardiograms in adults and children.
Identify if your PageWriter TC30 has the Government Bundle, Product 860354, and software revisions up to A.07.05.22.
The batteries may overheat, melt the device casing, and cause fire, which could injure patients or nearby users.
Check for the PageWriter TC30 with trolley Government Bundle, Product 860354, and software revisions up to A.07.05.22.
The recall record does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0859-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-0859-2019 from Philips. 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.
