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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Teleflex medical has been notified by their supplier of a premature "low sensor" indication on the internal oxygen sensor catalog number number #5804. the defect will prematurely indicate a "low sensor" causing the end user to conduct preventative maintenance earlier than earlier than necessary.