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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Customer complaint received that during troubleshooting a syringe filled with ez kleen was connected to the perox 2 reagent tubing. the ez kleen sprayed onto the operator's forehead after the syringe plunger caused the tygon tubing to disconnect at the check valve.