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 is recalling the hudson rci/performed uncuffed tracheal tube nasal due to incorrect product labeling. the affected product packaging is incorrectly labeled as being a "cuffed oral et tube." the correct product labeling is "uncuffed nasal et tube.".