Philips recalls PageWriter TC30 cardiograph devices with end-of-life batteries that may overheat, melt, or ignite causing injury. Affected units sold with software revisions up to A.07.05.22.
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 that may have batteries reaching end-of-life. These batteries can overheat, melt the device, or ignite, potentially injuring patients or nearby users.
Batteries that have reached end-of-life may overheat, causing the device case to melt and potentially ignite. This poses a fire risk to patients and people nearby during medical use.
Healthcare providers using Philips PageWriter TC30 cardiograph devices with end-of-life batteries are most at risk. Patients and others nearby could be injured if the device overheats or ignites.
Check for PageWriter TC30 cardiograph devices without trolley in government bundles. Look for software revisions up to and including A.07.05.22 on the device.
Verify the software revision on your PageWriter TC30 device; affected units have revisions up to A.07.05.22.
Reach out to Philips for assistance with the recall process or to determine if your device is affected.
Batteries that have reached end-of-life may overheat, causing the device case to melt and/or ignite, which can injure patients or nearby users.
Check for PageWriter TC30 cardiograph devices without trolley in government bundles with software revisions up to A.07.05.22.
Contact Philips for assistance with the recall process or to determine if your device is affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0861-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-0861-2019 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.
