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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Bd has recently confirmed low level contamination of listeria monocytogenes on the listed lots of non-sterile prepared plated media containing sheep blood. bd has identified the source of the listeria contamination as sheep blood used in the manufacture of prepared media.