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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Failure of the viking m lift as it relates to the control box (cbl 20)and the battery (bal 20). the product will stop functioning. note that there is a mechanical means to safely lower the patient during transfer.