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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Baxter that they have initiated a recall of various lots of buretrol solution sets (component 2c7564-buretrol solution set with 150ml interlink burette) which are found in the presource kit. this action has been initiated due to complaints for separation between the burette chamber and the drip chamber.