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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Conmed has received complaints of cervical cup or uterine balloon detachment for the vcare vaginal-cervical ahluwalia's retractor-elevators manufactured after april 11 2008 which may be related to user technique.
Model Catalog: 60-6085-100 (Lot serial: LOT 090120X - 090731X); Model Catalog: 60-6085-102 (Lot serial: LOT 090120X - 090731X); Model Catalog: 60-6085-101 (Lot serial: LOT 090120X - 090731X)