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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Manufacturer has identified compromises in sterile packaging that may allow a breach of the package's sterile barrier and may compromise the sterility of the product. the breach may not be easily seen. manufacturer has not received any complaints of injury associated with compromised sterile packaging. however it is possible that use of non-sterile product may introduce microbes and increase the potential for postoperative infection.