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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Software doit etre mis a niveau car il peut faire redemarrer l'apareil lorsque certaines conditions sont reunies.
Model Catalog: (Lot serial: c.0software with option); Model Catalog: (Lot serial: a74/a84 if notc79 or option); Model Catalog: (Lot serial: a76/a86 and not j26)