Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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Philips has received reports that speakers on the philips intellivue x2 and mp2 patient monitors have failed prematurely. this failure may be identified by the display of a "speaker malfunct." inop or by the absence of audible sound. speaker failures may delay recognition of an alarm condition if operators do not recognize that there is no alarm sound from the monitor and the monitor is not connected to another audible alarm annunciation system e.G. another bedside monitor or a central monitoring station.