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 dxh 800 dxh 600 and dxh slidemaker stainer may fail to notify the user of warnings or error conditions for low or depleted reagent conditions daily checks failures lis disconnection and printer failures at: - the alert status icon(s) on the system manager - the audible alarm at the system manager - the instrument beacon on the specimen processing module or slidemaker stainer the failure may occur when the system manager application is restarted or powered off/on.