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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Baxter has received complaints for opened pouches of minicap contained within the shipping carton of product code 5c4466p (lot #gd893891). baxter has determined the opened pouches were due to an incomplete seal. an incomplete seal may result in the povidone-iodine drying off within the minicap and becoming an ineffective disinfectant.