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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Bard access systems has become aware that a specific lot of statlock catheter stabilization device single unit pouches was released without unique product identifiers including product description package contents product code lot number and expiration date. the product was distributed in cases of 50 unit pouches. the case label is correct and complete. product return is not required.