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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Baxter has received complaints indicating that the sponge of the minicap was fully separated from the cap protruding from the cap or missing. use of an affected device may increase the risk of peritonitis. this is an imporant product information communication in which customers can arrange for replacement product where appropriate.