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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Siemens healthcare diagnostics identified the potential for an accelerated decline in counts per second (cps) for the immulite/immulite 1000 folic acid (lkfo1) kit lots 335 336 and 337. this may lead to a failed adjustment before the expiration date which is indicated on the kit label is reached.