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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Bard peripheral vascular (bpv) has confirmed that some devices from a specific lot (rewe1689) of product code mn1410 may contain an incorrect (longer) needle length than the size stated on the label. a small number of needles from the lot number specified which should be 10cm were instead 13cm.