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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Angiodynamics inc. (dba navilyst medical. inc.) the manufacturer of the xcela picc with pasv technology convenience kit for centenary hospital (4f single lumen) is conducting a medical device recall to the end user level. angiodynamics has determined that the affected product contains an inaccurate product description on the labelling the product is labelled as 5f - 55cm and the product is actually 4f - 55cm. angiodynamics began distributing product affected by this recall on july 14 2017.