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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Synthes (canada) ltd. is initiating a voluntary recall of the affected part number 249.926 lot number 8093100 for the synthes 2.4mm lc-dcp plate 6 holes 51mm. this recall is being initiated following synthes' receipt of a complaint regarding a screw being found in a package labeled for a 2.4 mm lc-dcp plate. the potential hazard of the presence of a screw in a package that should contain a plate does not pose the risk of harm to a patient. as the device is non-sterile and packaged in a clear bag the component will be easily recognizable as the incorrect part.