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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Patient sample database on the bactec fx are sometimes found to be unusable upon rebooting the instrument. the reboot proceeds normally until it tries to load the database file at which point the instrument reboots and then repeats this cycle indefinitely or customers see a message on the display that says "please insert a bootable device". the system will continue to agitate and incubate the samples.