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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The sterilization of the product is not performed according to iso 11135 standards. coloplast is not able to guarantee the sterility of the product.
Model Catalog: (Lot serial: ASP 150); Model Catalog: (Lot serial: ASP 145); Model Catalog: (Lot serial: ASP 105); Model Catalog: (Lot serial: ASP 125); Model Catalog: (Lot serial: ASP 110); Model Catalog: (Lot serial: ASP 135); Model Catalog: (Lot serial: ASP 165); Model Catalog: (Lot serial: ASP 155); Model Catalog: (Lot serial: AST TUBING); Model Catalog: (Lot serial: ASP 180); Model Catalog: (Lot serial: ASP 170)