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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Some immunocap products can have stoppers which might get detached. loosening of stoppers can be caused by shaking of the immunocap carrier during transport or when manually handled. in this case the red plastic weight can push the stopper partially out of the carrier or even open the carrier. a stopper sticking out of the carrier can lead to problems with the phadia 250 carrier handling and can lead to an error message and error marked carrier.