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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An increased trend in reports of keypad issues occurring during implementation or shortly after being placed in use. short circuits in the keypad may make pump inoperable or pump may not respond to keystrokes.