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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A small number of failures (0.85%) have been reported where components have cracked unexpectedly both at the fitting stage and after a period of use. similar failures could result in the limb wearer falling and injuring themselves.
Model Catalog: 409028 (Lot serial: S001 TO S365); Model Catalog: 409054 (Lot serial: R001 TO R365); Model Catalog: 409028 (Lot serial: R001 TO R365); Model Catalog: 409054 (Lot serial: Q001 TO Q365); Model Catalog: 409054 (Lot serial: S001 TO S365); Model Catalog: 409054 (Lot serial: P265 TO P365); Model Catalog: 409028 (Lot serial: P265 TO P365); Model Catalog: 409054 (Lot serial: T001 TO T048); Model Catalog: 409028 (Lot serial: T001 TO T048); Model Catalog: 409028 (Lot serial: Q001 TO Q365)