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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Unexpected positive reactions with the negative control.
Model Catalog: (Lot serial: LOT 221370 IS PACKAGE SYSTEMS); Model Catalog: (Lot serial: 33993); Model Catalog: (Lot serial: 33994); Model Catalog: (Lot serial: 33993 TO 33997); Model Catalog: (Lot serial: 33999 AND 33005)