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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Bd received 181 incidents in usa of clogged needles for batch 905615. needle is part of genentech's lucentis kits. lucentis is administered as an intravitreal injection (into the eye). the medication is drawn up through a 19 gauge filter needle and then the 30 gauge needle. the clogs were found prior to use.