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 identified risk with the alaris pk syringe pump that resulted in a situation where the near end of infusion (neoi) audible alarm on the 8005tig01 pk syringe pumps was not heard and/or not recognized by the clinician.