Philips IntelliVue MP2 patient monitor recall: Class II Recall
MedSun: Newsletter #54, November 2010

FDA Recalls

Speakers on the Philips IntelliVue X2 and MP2 patient monitors may fail, causing absence of an audible alarm and delaying patient treatment. The following MedSun-reported event occurred in the Emergency Room (ER) and is relevant to HeartNet clinical areas.

MedSun has received reports with this device. To read the event, please see the link provided in Additional Information below.

Additional Information:

FDA Recalls. Philips IntelliVue MP2 patient monitor recall: Class II Recall. September 29, 2010.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=94173&CREATE_DT=2010-09-29

MedSun Report. August 30, 2010.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/medsun/medsun_details.cfm?ID=%25%22%5DW%3B%27%5FH%20%0A&CFID=50094208&CFTOKEN=99b71ffe191c9bc9-AB37E


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