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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Bd medical has issued a recall on the bd insyte autoguard catheter cat. nos. 381433 and 38134 due to potential damage along the body of the catheter. a damaged catheter may lead to catheter leakage and the subsequent need for insertion of another catheter. the bd insyte catheter is a component in the medline maxillofacial pack dynj37293a.