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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Through our post-market surveillance program we have identified that a small quantity of the zoll pedi-padz solid gel multi-function electrodes (part numbers 8900-3000-01 and 8900-3001-01) manufactured in april 2015 (lot number 1615) have been labelled with the wrong expiration date and part number.