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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During a review of records at the buffalo grove global technical services center in the u.S. it was determined that a service technician may have failed to perform the dielectric voltage withstand (hipot) test on colleague infusion pumps that were serviced between april 1 2008 and november 14 2008.