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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Cardiac science identified 65 reported early failures of contact resistance in the k302 relay of the g3 series aed product line over a 3 year time period ending may 2009. these failures occur within 200 days of shipment. the shipment date corresponds to the date at which the device is activated and an automated daily self-test begins.
Model Catalog: 9390A-501 (Lot serial: Serial # 4261144); Model Catalog: 9390A-501 (Lot serial: Serial # 4261411); Model Catalog: 9390A-501 (Lot serial: Serial # 4261416); Model Catalog: 9390A-501 (Lot serial: Serial # 4261417); Model Catalog: 9390A-501 (Lot serial: Serial # 4261123); Model Catalog: 9390A-501 (Lot serial: Serial # 4261383); Model Catalog: 9390A-501 (Lot serial: Serial # 4261387); Model Catalog: 9390A-501 (Lot serial: Serial # 4261403); Model Catalog: 9390A-501 (Lot serial: Serial # 4261408)