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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Siemens healthcare diagnostics has confirmed that a small percentage of bead packs may intermittently fail to dispense a bead as a result of an issue with the bead pack plunger assembly. through the investigation of customer complaints and in collaboration with our supplier the frequency of occurrence has been determined as approximately 0.02%.