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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Coopersurgical is voluntarily recalling the milex omniflex diaphragm - size 80 p/n mxwfbo lot 153309. coopersurgical quality assurance program identified a size 80 labeled box was incorrectly packaged with a size 85 diaphragm.