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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By fully actuating the lever of the extension device handle skin can enter a gap between the handle lever and a recess in the handle bar. when the lever is released skin which might be within the gap could be pinched or cut.
Model Catalog: 1433.62A0 (Lot serial: Part 1433.62A0 All SNs); Model Catalog: 1433.62A1 (Lot serial: Part 1433.62A1 SN 1 to 90); Model Catalog: 1433.62A0 (Lot serial: Part 1433.62A1 SN 1 to 90); Model Catalog: 1433.62A1 (Lot serial: Part 1433.62A0 All SNs)