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
Potential for the packaging of the device to become damaged during packaging. this could lead to compromising the sterility of the product which increases the risk to the patient.
Model Catalog: 78050 (Lot serial: ALL(EXPIRATION DATING FROM); Model Catalog: 78050 (Lot serial: MAY 2010 TO MARCH 2015)); Model Catalog: 78050 (Lot serial: Model # 78050)