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 is conducting a recall of the bd interlink threaded lock cannula. this recall has been initiated due to the potential for a small percentage of the lot to exhibit open seals. this adversely impacts unit package integrity and product sterility. bd has determined that there is a very low level of risk since most of the open seals are visible to the user. a decision was made to remove this lot from the market as a precautionary measure.