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 a result of a software limitation in some cases when an extra wash is applied to sample probes before switching sample types either an inside or an outside probe is not properly washed. in such a case a probe is not washed with wash solution (detergent-1 or/and detergent-2) but washed only with water.