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 notifying customers of an incompatible product that should not be used with specific one-link devices. customers have reported no-flow and restricted flow situations when attempting to connect the microclave device to the male luer lock adapter of the one-link catheter extension set in product code 7n8371. baxter's investigation has determined that the microclave dimensions are not compatible with the iso-compliant male luer lock adapter dimensions of the affected one-link product codes. under-infusion or interruption of therapy could result.