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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Several lots of the beaver 4.0mm banana blade are experiencing brittle fracture. a number of product complaints were received with this indication noted during surgery. in the event that the blade breaks and falls into the patient it could potentially be difficult to retrieve and may lead to a surgical delay.