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.
데이터 추가 비고
원인
An extension of hc#50115 recall. after filing report 50115 further reports emerged of additional customer experiences for fracturing cannulas that were from different c0r36 lots as well as from model c0r37.
Model Catalog: C0R37 (Lot serial: >10 lot numbers. Contact); Model Catalog: C0R36 (Lot serial: >10 lot numbers. Contact); Model Catalog: C0R36 (Lot serial: manufacturer.); Model Catalog: C0R37 (Lot serial: manufacturer.)