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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Immucor inc. is issuing a product recall notification for capture-r ready-screen (3) lot r889. lot r889 demonstrates an increased trend of complaints for unexpected negative/false-negative antibody screen results. in post-release testing the product continues to demonstrate appropriate positive reactivity with antigen-positive test wells.