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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Bd has determined that if the undo function is used to undo a gate deletion the statistical results may be mismatched. as this may not be obvious to the user the user may not realize the incorrect results.
Model Catalog: 339455 (Lot serial: VER 4.0.2 TO 5.2.1); Model Catalog: 343926 (Lot serial: VER 4.0.2 TO 5.2.1); Model Catalog: 343928 (Lot serial: VER 4.0.2 TO 5.2.1); Model Catalog: 347527 (Lot serial: VER 4.0.2 TO 5.2.1); Model Catalog: 347526 (Lot serial: VER 4.0.2 TO 5.2.1)