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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Ortho clinical diagnostics (ortho) has initiated this recall pertaining to engen systems configured with a thermo scientific centrifuge module and tcautomation (tca) software versions 3.6.1 and below. ortho became aware of one confirmed instance of test results that were mis-associated with the wrong sample id (sid) and were reported prior to the engen system detecting the sid mismatch. assay results are potentially associated with the wrong patient and reported out of the laboratory. this could lead to inappropriate intervention with the potential for serious injury to the patient. ortho received no reports of patient injury due to this issue.