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
Trays were shipped to customers containing lidocaine which have gmp issues in the us by mistake some of thes trays were shipped to customers.
Model Catalog: P4340A (Lot serial: ALL LOTS WITHOUT YELLOW); Model Catalog: P4341B (Lot serial: ALL LOTS WITHOUT YELLOW); Model Catalog: P4341B (Lot serial: STICKER ON CASE AND TRAYS); Model Catalog: P4340A (Lot serial: STICKER ON CASE AND TRAYS); Model Catalog: 4325 (Lot serial: ALL LOTS WITHOUT YELLOW); Model Catalog: 4325 (Lot serial: ON STICKER AND TRAY)