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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These custom procedure packs contain the cardinal medi-vac non-conductive suction tubing that has been recalled by cardinal health. medline industries was alerted by cardinal regarding a product recall for their sterile medi-vac non-conductive suction tubing due to the possibility that packaging seals may be compromised.