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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Del medical have determined that in rare cases a fastener within the internal counterbalance system may fail. in the event of a fastener failure the wallstand image receptor will descend to the lowest position and cannot be used for x-ray examination until repairs are completed.