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 devices were shipped with an incorrect configuration file disarming the 'flashing red x' and audible alarms when they are powered by ac or dc power and have no battery or low battery capacity. this also causes a weekly self diagnostic test to run hourly depleting batteries faster than normal when stored without an external power source.
Model Catalog: M3536A (Lot serial: US00533518 - US00535118); Model Catalog: M3535A (Lot serial: Serial numbers); Model Catalog: M3536A (Lot serial: Serial numbers); Model Catalog: M3535A (Lot serial: US00533518 - US00535118)