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
Enzymatic method, ammonia - Product Code JIF
원인
Results for ammonia are below the linear range of the assay for samples that have been collected in sodium or lithium heparin tubes.
조치
Sentinel Urgent Field Safety Notice issued on 9/22/15 by Abbott to customers, including their US customers.
Actions to be Taken
1. Immediately discontinue use of lot 50083Y600 and destroy any remaining inventory.
2. Order a replacement Ammonia Ultra reagent lot.
3. Follow your individual laboratory protocol regarding reviewing previously reported patient results.
4. Please retain this communication for future reference. If you have forwarded any MULTIGENT Ammonia Ultra reagent lot 50083Y600 to another laboratory, please provide a copy of this letter to them.
Contacts
If you or any of the health care providers you serve have any questions regarding this information, U.S. Customers should contact Customer Service at 1-877-4 ABBOTT.
Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.