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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If a test with a known result is inserted in a patient request via a connection or manually via erm and this test contains a rule... this defect could affect patient results and could cause improper diagnosis.
Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V03.13.1 all UNIX); Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V03.12.B all UNIX); Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V05.01.B all UNIX); Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V05.02.1 all UNIX); Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V11.01.1 all UNIX); Model Catalog: TD-SYN-01 (Lot serial: TDLims V21.04.1 for HP-UX AIX); Model Catalog: TD-SYN-01 (Lot serial: TDLims V22.02.1 for AIX SunOS); Model Catalog: TD-SYN-01 (Lot serial: TD-Synergy V11.11.1 all UNIX)