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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This recall has been initiated due to product below specified hardness. the tubes are too pliable and would be difficult to use for intubation. there is a possibility that the tube could fold over in the narrower areas of assembly. supplier of lts-d products noted in their process and informed king systems on jan 21 2011.