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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Smith & nephew has initiated a product recall of select lots of the mosaicplasty dp disposable harvesting system due to a packaging issue. it has been identified that it is possible for the devices to dislodge from the packaging tray during shipment potentially compromising the sterile barrier. the mosaicplasty dp system is used osteochondral grafting procedures.