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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Mercury medical has issued field safety notice due to the potential of a silicone mask with a 15 mm male port being able to be forcibly inserted into the protective cap covering the opening of the t-piece circuit. incorrect use of the product in this way will result in complete occlusion of the patient circuit and consequent failure to ventilate the patient resulting in hypoxia or delay in patient care.