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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Bulk-packaged rolls of micropore surgical tape may exhibit the same inconsistent performance that was observed with single use rolls recalled (recall number 53073) if used as the primary securement device for dialysis needles or pressure dressings used after dialysis treatments. only the identified lots were imported by 3m canada.