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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To provide clarification about the packaging configuration of the products. products are packaged with a double sequential sterile wrap and placed into an outer dust cover. the dust cover is secured with the package label. the label on the outer package denotes the product as being sterile. the chest drain inside the packaging is sterile but the outer dust cover is not sterile.
Model Catalog: 3600-100 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2012-320 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2002-400 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2002-300 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2002-000 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 4020-100N (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 4000-100N (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 16400 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 3612-400 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 3650-100 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 3620-100 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 3612-100 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2050-000 (Lot serial: Lots expiring before Oct. 2019); Model Catalog: 2002-100 (Lot serial: Lots expiring before Oct. 2019)