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
Subsequent to tissue release, cryolife received new information related to the donor time of death, which caused the donor to no longer meet cryolife's acceptance criteria for warm ischemic time.
조치
Consignees were notified by telephone on May 17, 2005. Both tissues were returned and destroyed.