Philips recalls IntelliVue MP80 monitors (model M8008A) due to potential failure to alarm. Affected units may not alert users to critical health changes, posing a risk of serious injury.
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue MP80 monitors (model M8008A) because they may not alarm when a patient's condition worsens. This could lead to serious injury or death if the monitor fails to alert healthcare providers.
The monitors may not sound an alarm when a patient's condition deteriorates, which could delay critical medical intervention. This risk is specific to healthcare settings where continuous monitoring is essential.
Healthcare providers using the IntelliVue MP80 monitors are most at risk. Patients in critical care settings may be affected if the monitor fails to alert medical staff.
Check for the product number M8008A on the monitor. The recall includes all units sold with this model number.
Look for the product number M8008A on the monitor's label.
The monitors may not alarm when a patient's condition worsens, which could delay critical medical intervention.
Check for the product number M8008A on the monitor's label.
The recall does not specify a remedy, so contact Philips directly for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0857-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0857-2026 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.
