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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Due to a geometrical incompatibilty between the light guide cable and light source the "high intensity mode" cannot be switched on. due to a production failure of the manufacturing partner the distance between the coverglass of the light guide cable and the ledge does not meet specifications. production between january 2009 and may 28 2009 was affected.
Model Catalog: A50021A (Lot serial: ALL LOTS (09/01/01-09/05/28)); Model Catalog: A50003A (Lot serial: ALL LOTS (09/01/01-09/05/28)); Model Catalog: A50001A (Lot serial: ALL LOTS (09/01/01-09/05/28)); Model Catalog: WA50003L (Lot serial: ALL LOTS (09/01/01-09/05/28)); Model Catalog: A50023A (Lot serial: ALL LOTS (09/01/01-09/05/28))