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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B-l recently determined that posterior fluidics modules installed in the stellaris pc vision enhancement systems by the b-l field service organization between january 3 2012 and august 8 2012 may need to be recalibrated. these modules which regulate the performance of the vitrectomy probe may exhibit behavior that could result in less efficient aspiration.