medical Class II Updated 2020-12-16

Philips North America Llc recalls Philips IntelliVue MP2 Patient Monitors (865040) - Product U

Recalled Product

Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside of the hospital environment.


Hazard / Issue

Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the display of a Speaker Malfunct. INOP or by the absence of audible sound, may result in delayed treatment of the patient.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Serial Numbers: DE73602213 DE73602577 UDI: (01)00884838000278(21)DE73602213 (01)00884838000278(21)DE73602577
View official government recall

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