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. received notification from its supplier synthes gmbh that a medical device recall was being initiated for part number(05.001.046) lot number (8230998) due to incorrect labelling of the device. this voluntary recall of the burr attachment m is used with synthes electric pen drive and air pen drive systems. one delivery of burr attachment l were marked with the marking of an "m" and that burr attachment m were marked with the marking of an "l".