Philips recalls PageWriter TC70 w/trolley Government Bundle (Product 860352) with software revisions up to A.07.05.22 due to risk of battery overheating, melting, and fire causing injury to patients or users.
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 TC70 w/trolley Government Bundle devices with specific software versions because their batteries may overheat, melt, or ignite. This poses a risk of injury to patients or people nearby if the device is used improperly.
The batteries in these devices may reach the end of their life and overheat, causing the device casing to melt and potentially ignite. This fire hazard could injure patients or people in close proximity during use.
Healthcare professionals using the PageWriter TC70 w/trolley Government Bundle for electrocardiogram readings are most at risk. Patients and others nearby could be injured if the device overheats or ignites.
Check for the PageWriter TC70 w/trolley Government Bundle with product number 860352 and software revisions up to A.07.05.22. The device is used for evaluating electrocardiograms in adults and pediatric patients.
Verify if your device has product number 860352 and software revisions up to A.07.05.22.
Reach out to Philips for guidance on next steps if you have the recalled device.
Philips recalls these devices because their batteries may overheat, melt, or ignite, posing a risk of injury to patients or nearby users.
Check if your device has product number 860352 and software revisions up to A.07.05.22. Contact Philips for further instructions.
Yes, if the device overheats or ignites, it could cause injury to patients or people nearby.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0857-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-0857-2019 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.
