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
Safety advisory regarding use of the "evaluation/magnify" function.
Model Catalog: (Lot serial: Model # 27 91 023 SN 14024); Model Catalog: (Lot serial: Model # 27 91 023 SN 13105); Model Catalog: (Lot serial: Model # 27 91 023 SN 14054); Model Catalog: (Lot serial: Model # 27 91 023 SN 14674); Model Catalog: (Lot serial: Model # 27 91 023 SN 14807); Model Catalog: (Lot serial: Model # 27 91 023 SN 14617)