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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Arrow has issued a recall for these products due to potential packaging damage. therefore the sterility of the product cannot be guaranteed. if a non-sterile product is used there is potential for infection to occur. no patient injuries have been reported related to this issue.