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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A complaint investigation has identified instances of labelling errors for a specific component in the mach 4 universal hrp-polymer kit. a recall is being initiated to facilitate a field correction that could be necessary for the mach 4 mouse probe vial within the mach 4 universal hrp-polymer kit. it may be incorrectly labelled as mach 4 hrp-polymer.