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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Potential for a sample misidentification on the acl top family that only occurs following a specific set of steps combined with inability of the system to read a specific sample rack barcode.
Model Catalog: 0000280010 (Lot serial: SN 09080100 to 14050732); Model Catalog: 0000280030 (Lot serial: SN 06020101 to 10080662); Model Catalog: 0000280050 (Lot serial: SN 09120101 to 14050368); Model Catalog: 0000280040 (Lot serial: SN 08010100 to 14052901); Model Catalog: 0000280000 (Lot serial: SN 03110101 to 11111174); Model Catalog: 0000280020 (Lot serial: SN 03110101 to 11111174); Model Catalog: 0000280030 (Lot serial: SN 03110101 to 11111174); Model Catalog: 0000280000 (Lot serial: SN 06020101 to 10080662); Model Catalog: 0000280020 (Lot serial: SN 06020101 to 10080662); Model Catalog: 0000280000 (Lot serial: SN 08120100 to 14050198); Model Catalog: 0000280020 (Lot serial: SN 08120100 to 14050198); Model Catalog: 0000280030 (Lot serial: SN 08120100 to 14050198); Model Catalog: 0000280060 (Lot serial: SN 11110101 to 14051302)