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 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.
The IntelliVue monitors may not alarm as intended, which could lead to undetected patient distress. This defect presents a high hazard level, as timely alarms are critical for patient care.
As of the recall date, there are no reported incidents or injuries associated with this defect. However, the potential for serious harm exists if alarms fail to alert healthcare providers.
Stop using the IntelliVue MP30 monitors immediately. Contact Philips North America or your healthcare provider for further instructions regarding the recall.
For more information, contact Philips North America at 1-800-xxx-xxxx or visit the recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-0852-2026.
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