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 corporation has been notified by nipro medical corporation of a product recall for specific lots of nipro bloodline code a230tr/v810tr. the mini clamp used on the venous transducer protector line was manufactured from materials not suitable for gamma radiation sterilization. baxter has received complaints of breaking mini clamp on the venous transducer protector line.