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, more than minimally manipulated allograft - Product Code OHA
원인
Devices, which met fda and aatb eligibility criteria, were distributed. final autopsy and toxicology reports indicated the presence of morphine in the urine.
조치
The firm notified the consignees by letter on 05/14/2018.