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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It was reported to stryker sustainability solutions that the tip of two angiographic catheter's model # 10732203 broke off prior to being used on the patient. during the complaint investigation visual inspection confirmed that each device had fractured near the distal tip.