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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There is the potential for misconnecting or miskeying the electrical connector (between the head motor extension cable and the foot section) during initial set-up or installation of the product. this results in immediate and permanent failure on first use and has the potential to cause a fire.
Model Catalog: BARPKGIVC-1633 (Lot serial: 01Fxxxxxx to 11KF024680); Model Catalog: BARPKG (Lot serial: 01Fxxxxxx to 11KF024680); Model Catalog: BARPKGCA (Lot serial: 01Fxxxxxx to 11KF024680); Model Catalog: BAR600IVC (Lot serial: 01Fxxxxxx to 11KF024680); Model Catalog: BAR600 (Lot serial: 01Fxxxxxx to 11KF024680)