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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During internal investigation our manufacturer confirmed a possible software issue where the strips cassettes (cobas upack) on cobas u601 urinalysis system is denied by the user software although the expiry date has not been reached. this is true for every month reaching the cassette expiry date.