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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Leica biosystems recently became aware that there is a potential issue with the bond oracle her ihc system ta9145 lot numbers 12135 and 13341. they have become aware of a potential occurrence of over-staining on procedural control cell-lines that are supplied as part of the system. there is the possibility that the over-staining may be observed in in-house tissue controls and/or patient tissue.