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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One vigilance case & 2 complaints were received in 2008 in relation to the philips catheter 1 eye female metric thread. the metallic tip detached from the shaft upon or prior to using the device.