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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The central wire may be undersized which could cause it to disengage during removal.
Model Catalog: (Lot serial: 475.050 AND 475.242 TO 475.250); Model Catalog: (Lot serial: PART NUMBERS 475.042 TO); Model Catalog: (Lot serial: ALL LOT NUMBERS)