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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On some acuson s2000 systems with abvs options the edges on the inside of the transducer pod may not be competely deburred to avoid sharp edges. a potential risk exists that an operator could sustain a cut when touching the sharp edge while cleaning the inside of the pod.