Philips North America recalled 1,913,441 IntelliVue MP2 monitors on October 31, 2025. The monitors may not alarm as intended, posing a risk to patient safety. Affected devices were distributed worldwide, including the United States and multiple countries.
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 recalled product is the IntelliVue MP2, Product Number: M8102A. The device was sold worldwide, including the US, from an unspecified start date until the recall date. Pricing information is not provided.
The IntelliVue monitors may not alarm, which can lead to undetected patient emergencies. This defect poses a high risk to patient safety and requires immediate attention from healthcare providers.
There are no specific reported incidents or injuries noted in the recall information. The potential failure of the alarm system represents a serious concern.
Stop using the IntelliVue MP2 monitor immediately. Follow the recall instructions provided by Philips North America and contact your healthcare provider for further guidance.
For more information, visit the FDA website at www.accessdata.fda.gov or contact Philips North America. They have issued notification letters to affected users.
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