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 device is now contraindicated for use in ligating the renal artery during laparoscopic donor nephrectomies as the device may become dislodged. devices to be relabelled with new contraindication.
Model Catalog: 543965 (Lot serial: ALL LOTS); Model Catalog: 544240 (Lot serial: ALL LOTS); Model Catalog: 544230 (Lot serial: ALL LOTS); Model Catalog: 544250 (Lot serial: ALL LOTS)