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
Supplement, culture media - Product Code JSK
원인
Recalled product may not provide adequate recovery of legionella pneumophila when used as directed and may result in false negative identification of legionella pneumophila.
조치
Thermo Fisher sent an Urgent Medical Device Recall letter dated October 17, 2014, to all affected customers.