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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Ocd has issued a recall pertaining to a potential malfunction in a wire connector used in the vitros 4600 vitros 5600 and vitros 51 fs systems that were shipped during a specific date range. to date six customers reported the smell of melting plastic or observed smoke originating from their vitros 4600 and 5600 systems. although reports are confined to the vitros 4600 and 5600 systems the same wire connector is also used on vitros 51 fs systems. as a precaution ocd is contacting customers to notify them of this potential malfunction for vitros systems that were shipped during a specific date range.