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.
데이터 추가 비고
원인
Since issuing a recall in december 2008 smiths medical has found that one lot of keypads in some fully assembled pumps and some kits is predisposed to short circuits which can render the keypad inoperable.