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 become aware that the heartstart mrx defibrillator/monitor can be susceptible to one or both of the issues described below. 1. the co2 inlet port associated with end-tidal carbon dioxide (etco2) monitoring on mrx monitor/defibrillators can be pushed into the mrx housing making it inaccessible. this can occur if the user attempts to push the co2 filterline fitting into the inlet port instead of twisting it clockwise as described in the mrx instructions for use. 2. the handle can separate from the mrx housing due to breakage of mounts on the rear case.