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
Siemens has issued an urgent field safety notice to inform customers of potential when both ports (serial and ethernet) are configured to transmit data the data stream from one port could potentially affect the data stream from the other port. this could cause the message received by the lis (data management system) to include either: duplicate data missing data data from a different patient. siemens has not observed this scenario and the expected frequency of occurrence is extremely unlikely. if this issue occurs only one analyte has the potential to be affected (i.E. if a panel of analytes is ordered only one could be affected).