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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Fertipro decided to remove all the spermmar iga kits with brown beads of the following batches from the marker: fp14a09 fp14a10 fp14a11. note that this recall is not related to an incident. there is no possibility for physical harm deterioation of health or death in the user or patient.