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 pack contains a vacutainer manufactured by bd. the bd lav top vacutainer k2 plus blood collection tube is recalled by bd because some lots were manufactured with insufficient edta additive. according to bd insufficient edta additive could lead to erroneous results. lots 15wb7898 and 15wb9865 of medline pack dynj41766a contain one of the affected bd vacutainers catalogue number 367844 lot. no. 5154624.