U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Heart-Valve, Allograft - Product Code MIE
원인
During a retrospective review, cryolife noted that the donor tissue exceeded the acceptable warm ischemic time when utilizing the 'last seen alive' time in their calculation.
조치
Consignees were notified by letters dated 12/17/2004, 01/03/2005 and 01/19/2005.