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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The product under recall is the dbp2800 battery pack which is used to power the ddu100 semiautomatic external defibrillator (aed). in rare instances when the aed is used with an affected battery pack the aed may falsely detect an error condition cancel charge and not provide therapy. this situation can occur only with dbp-2800 battery packs shipped prior to june 4 2007. although the probability of this condition is very low as a precaution defibtech is correcting all potentially affected batteries. no occurrences have been reported in canada.