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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Some of the needles were displaced or projected out of the protective cap when the user opened the casing of the multi sample blood collecting needle for lot number 130908 only. the patient needle should remain in the cap after the casing is opened.