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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Potential for the male swab to present a defectiveness where the cotton head of the swab may dislodge and/or unravel with minimal force. this could result in having cotton fibers remaining within the urethra during specimen collection of male patients.