Philips North America is recalling 1,913,441 IntelliVue MP2 patient monitors worldwide. The devices may fail to alarm when critical conditions arise. Hospitals should stop using the monitors and follow Philips recall instructions.
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 MP2 is a patient monitor used in hospital settings to track vital signs and alert clinicians to changes in patient status.
If the monitor fails to alarm, clinicians may miss critical events, delaying intervention and potentially compromising patient safety.
This recall is not part of a broader industry pattern.
Hospitals may need to replace or repair affected monitors, adjust monitoring protocols, and implement temporary solutions to ensure patient safety.
Examine the device label and packaging for model, UDI-DI, and serial number information
Replacement or remediation timelines typically 4-8 weeks, depending on hospital procurement and Philips processes
Document recall notice, device identifiers (model, UDI-DI, serial numbers), and communications with Philips for records
Model numbers: M8102A. UDI-DI: 00884838000278. All Serial Numbers affected. Sold to healthcare facilities worldwide, including US nationwide. When sold: Unknown. Price: Unknown.
No injuries or incidents have been reported.
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