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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Baylis medical company is recalling lots of protrack microcatheter due to the possibility that the catheter may have circumferential defects along its shaft. if the affected device is used for infusions there is a possibility of fluid leakage.