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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The z depth indicator angulated (dia 586) has incorrect depth indications. the first 30mm marking is correct however the following 4 markings have been manufactured with 4 mm distance instead of 5 mm.
Model Catalog: PART OF KIT 29162 (Lot serial: 35517 (kit 29162)); Model Catalog: DIA 586 (Lot serial: 35517 (kit 29162)); Model Catalog: PART OF KIT 29162 (Lot serial: 33451); Model Catalog: DIA 586 (Lot serial: 33451); Model Catalog: PART OF KIT 27136 (Lot serial: 35517 (kit 29162)); Model Catalog: DIA 586 (Lot serial: 31085 (kit 27136)); Model Catalog: PART OF KIT 29162 (Lot serial: 31085 (kit 27136)); Model Catalog: PART OF KIT 27136 (Lot serial: 31085 (kit 27136)); Model Catalog: PART OF KIT 27136 (Lot serial: 33451)