Philips North America recalled 1,913,441 IntelliVue MP30 monitors on October 31, 2025. The devices may fail to alarm, posing a serious risk to patients. Users must stop using the monitors and follow recall instructions immediately.
Potential issue where the IntelliVue monitors did not alarm.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips North America Llc or your healthcare provider for instructions. Notification method: Letter
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The IntelliVue MP30 monitor is a medical device used in healthcare settings to monitor patient vital signs. Healthcare providers rely on these monitors to receive timely alerts regarding patient conditions.
The monitors may fail to sound alarms when critical changes in patient condition occur, posing a risk to patient safety. Alarms are essential for alerting healthcare staff to emergencies and ensuring timely interventions.
This recall is not part of a broader industry pattern.
The failure of these monitors to alarm could lead to undetected patient distress, potentially resulting in serious health consequences. Immediate action is necessary to prevent risks associated with continued use.
The product number and UDI-DI can typically be found on the back or bottom of the monitor.
Expect a timeline of 4-6 weeks for processing refunds or replacements after returning the monitor.
Keep copies of any correspondence with Philips and document the return process, including photos of the monitor and the shipping receipt.
The recalled product is the IntelliVue MP30 with product number M8002A. These monitors were distributed worldwide, including the U.S. and over 100 other countries. No price information is available.
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