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 medical has received complaints regarding scales and/or bed exit systems on gobed gobed+rosebed and gobed ii. the units cited were manufactured between march 1 2002 and june 302008. our investigation identified that the reported issues could be attributed to load cell malfunctions.