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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Cryolife was notified by the tissue bank that recovered this donor tissue of inconsistenceies in the medical/social history interview. specifically one or more questions that were used in determining donor eligibility were either not asked of the donor family or was not appropriately asked.