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 increased number of leakages were reported due to over welded coils on the patient and drainage lines. this led to difficulties in unrolling the tubing set causing damage to the lines and possibility of leakage.