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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Spacelabs healthcare has identified an issue with model 91367 91369 91370 91387 & 91393 medical patient monitors equipped with the perioperative option (-d). one customer reported a safety concern over the inability to recognize the status of the monitor's audible alarms when the device has been left in the end case mode.