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.
데이터 추가 비고
원인
Under certain circumstances overheating and subsequent failure of the optotriac 25 amperes.
Model Catalog: (Lot serial: M/N INTEGRA); Model Catalog: (Lot serial: S/N 760100 TO S/N 760871); Model Catalog: (Lot serial: S/N 750100 TO S/N 759328); Model Catalog: (Lot serial: S/N 752804)