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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Vascutek is providing important user information regarding gelweave vascular prosthesis. currently vascutek provides a high temperature cautery with each gelweave vascular graft. vascutek have decided to stop supplying the cautery with these product packs due to the cautery battery having a shorter shelf life than the graft.
Model Catalog: 731224 (Lot serial: ALL LOTS); Model Catalog: 731222 (Lot serial: ALL LOTS); Model Catalog: 731220 (Lot serial: ALL LOTS); Model Catalog: 731218 (Lot serial: ALL LOTS); Model Catalog: 731034 (Lot serial: ALL LOTS); Model Catalog: 731032 (Lot serial: ALL LOTS); Model Catalog: 731030 (Lot serial: ALL LOTS); Model Catalog: 736038 (Lot serial: ALL LOTS); Model Catalog: 736034 (Lot serial: ALL LOTS); Model Catalog: 736032 (Lot serial: ALL LOTS); Model Catalog: 736030 (Lot serial: ALL LOTS); Model Catalog: 736028 (Lot serial: ALL LOTS); Model Catalog: 736026 (Lot serial: ALL LOTS); Model Catalog: 736024 (Lot serial: ALL LOTS); Model Catalog: 736022 (Lot serial: ALL LOTS); Model Catalog: 736016 (Lot serial: ALL LOTS); Model Catalog: 736014 (Lot serial: ALL LOTS); Model Catalog: 736010 (Lot serial: ALL LOTS); Model Catalog: 736008 (Lot serial: ALL LOTS); Model Catalog: 736006 (Lot serial: ALL LOTS); Model Catalog: 735034ST (Lot serial: ALL LOTS); Model Catalog: 735034 (Lot serial: ALL LOTS); Model Cat