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 has initiated an urgent product recall of the component 306553 the bd posiflusht saline flush syringe 10ml lots 4128353 3046276 and 3024261 since some unit packages may exhibit open seals which impacts package integrity and potentially product sterility. the syringes are found in these cardinal health presource kits.