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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The nibp pump inside of the module may come loose from its secured location and become suspended by the air hoses and electrical wiring. should this occur you may hear an unusual "rattling" noise coming from the module during anon-invasive blood pressure measurement or when the module is being handled or moved. in rare cases the module may cease to function. there have been no injuries associated with this issue.