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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During a routine shelf-life aging test a number of devices exhibited signs of damaged packaging which may lead to compromised sterility which has 30% chance of death as the contamination is on the bloodstream.
Model Catalog: HSK-2043 (Lot serial: 8030571 TO 9011671); Model Catalog: HSK-2038 (Lot serial: 8030372 TO 9012271); Model Catalog: HSK-2043 (Lot serial: 8030372 TO 9012271); Model Catalog: HSK-2038 (Lot serial: 8030571 TO 9011671)