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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Dale medical products inc. has identified an issue within some endotracheal tube holders (product# 270) manufactured between march and june of 2016. as a reminder these endotracheal tube holders contain the endotracheal tube holder itself along with an adhesive "faceplate" (individual product # 273). we have found that some et tube holders contain an adhesive faceplate that may lose its adhesive quality over time and therefore not perform as it should. by "over time" we mean while in storage awaiting use not after being applied.