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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An issue arising from our angled syringes containing 0.5-1mm 0.5cc and 1cc granules has come to our attention. it has been reported that post re-hydratation the syringe plunger could not always be pushed all the way leading to extrusion issues.