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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Bayer observed an increase in reports of device breakage for nova-t in 2015. the reported breakage was noticed during insertion or shortly after insertion in connection with expulsion of the t-body loop with attached threads.
Model Catalog: CU 200 AG (Lot serial: TU014KS); Model Catalog: CU 200 AG (Lot serial: TU013RK); Model Catalog: CU 200 AG (Lot serial: TU011WR); Model Catalog: CU 200 AG (Lot serial: TU0164H); Model Catalog: CU 200 AG (Lot serial: TU00Z67); Model Catalog: CU 200 AG (Lot serial: TU00VV7); Model Catalog: CU 200 AG (Lot serial: TU01108)