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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Medline has received a recall notice from conmed regarding their core reposable trumpet handpiece (conmed p/n cd8300). these handpieces are used as a component in several cds modules sold by medline canada. conmed is issuing this recall because the individual package seal may be compromised which could potentially affect the integrity of the sterile barrier. the handpieces are to be removed from the packs upon opening and discarded. the medline pack has been terminally sterilized therefore the remaining components within the pack are safe to use.