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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Due to the low radiopacity of the affected lots there is a possibility that the correct placement of the catheter be difficult to confirm by x-ray.
Model Catalog: (Lot serial: DEV LIC # 306); Model Catalog: (Lot serial: catalogue number g892); Model Catalog: (Lot serial: lots:72160VM73379VM74686VM)