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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This recall is being initiated due to an issue when validating a patient using a medical record number (mrn). this system is designed to allow data validation with an mrn only. if the user mistypes the patient mrn at the time of data entry the system could potentially overwrite the existing patient demographics or create an "unknown" patient.