Philips recalls IntelliVue MP2 monitors (product number M8102A) that may not alarm properly. This could lead to undetected medical emergencies. Affected units were sold from [date] to [date].
Potential issue where the IntelliVue monitors did not alarm.
Philips is recalling IntelliVue MP2 monitors that may not alarm properly, which could lead to undetected medical emergencies. This recall affects medical devices used in hospitals and clinics.
The monitors may not alarm when a medical emergency occurs, potentially missing critical health changes. This could lead to undetected medical emergencies if the monitor fails to alert healthcare providers.
Hospitals and clinics using Philips IntelliVue MP2 monitors are most at risk. Patients and staff could be affected if the monitor fails to alarm during critical medical events.
Check for product number M810: M8102A on the monitor. The recall includes all units sold with this product number.
Look for product number M8102A on the monitor's label.
The monitors may not alarm properly, which could lead to undetected medical emergencies.
Check for product number M8102A on the monitor. If you have this model, contact Philips for further instructions.
The recall states the monitors may not alarm properly, which could lead to undetected medical emergencies. However, the remedy is not specified in the record.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0849-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-0849-2026 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.
