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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Baxter corporation is initiating a lot-specific recall of some catheter extension sets and catheter extension set kits. the individual packages are distributed in strips separated by perforations. some customers have reported that when separating an individual package from its attached grouping the adjacent package has opened compromising its sterile barrier properties.