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
Multi calibrator diskette lot m002642g contains an error that will prevent synchron systems phosphorous reagent (phs ref a09426) from calibrating on synchron lx systems. phs will not calibrate and sample results cannot be generated after loading the diskette with the error which may cause a delay in reporting phosphate levels.