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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Conmed linvatec is voluntarily recalling selected serial numbers due to the front panel of the console containing incorrect artwork depicting a bf rating (man in box) per iec60601-1: medical electrical equipment: general requirements for basic safety and essential performance.