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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Film exhibits straight bands of fog readily identified artifact. the artifact could necessitate a repeat examination.
Model Catalog: 8999245 (Lot serial: LOT NUMBERS); Model Catalog: 8347098 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8931537 (Lot serial: LOT NUMBERS); Model Catalog: 8638041 (Lot serial: LOT NUMBERS); Model Catalog: 8347098 (Lot serial: LOT NUMBERS); Model Catalog: 8999245 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8931537 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8638041 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8126393 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8410789 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8408858 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8407710 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8341422 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8310286 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8301905 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8092421 (Lot serial: SEE 02 COMMENTS FOR AFFECTED); Model Catalog: 8063