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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Due to handles requiring batteries to operate it was determined the potential for insufficient contact causing inconsistent (intermittent or flickering) lighting was present for a small number of the handles. intermittent lighting may compromise the user's ability to visualise the patient's airway which may result in delayed treatment.