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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On february 14 southmedic received a customer complaint indicating a potential occlusion of the co2 sampling line on a southmedic capnography mask. inspection of current stock of the lot number in question did not identify any issues however investigation into additional lots manufactured with the same subassembly resulted in identification of occluded co2 sampling lines. subsequently all stock of various product skus manufactured with a co2 sampling line were placed on hold for further inspection.