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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Stryker instruments has become aware that certain lots of the stryker painpump2 and painpump2 blockaid have exhibited: 1)a high failure rate associated with a cracked port housing which leads to internal or external leaks. 2)a high failure rate associated with electronic failure which stems from a damaged capacitor on the electronic board assembly.