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.
데이터 추가 비고
원인
Based on complaints received from the field it was identified that certain control/calibrator products are missing some assay test codes. therefore no target values for the affected assays will be entered into the calibrator or control field when the barcode is scanned by the acl top family member. if a target value was entered on the instrument from a previous calibrator or control lot it will remain unchanged.