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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As part of market and product monitoring draegerwerk ag& co. kgaa the parent company of draeger medical canada inc. became aware that a batch of circuit boards with potentially faulty pressure sensors has been installed over a short period in early 2017 in oxylog 2000 plus and oxylog 3000 plus devices.