PlainRecalls
FDA Devices Moderate Class II Terminated

Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista System. Measurements are used as an aid in the management of heart, liver, and kidney transplant patients.

Reported: January 29, 2014 Initiated: December 5, 2013 #Z-0818-2014

Product Description

Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista System. Measurements are used as an aid in the management of heart, liver, and kidney transplant patients.

Reason for Recall

Complaints were received regarding variability in recovery of QC and patient results with certain lots of the Dimension Vista CSA Flex reagent cartridges.

Details

Units Affected
1586
Distribution
Worldwide Distribution - USA (nationwide) and Canada.
Location
Newark, DE

Frequently Asked Questions

What product was recalled?
Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista System. Measurements are used as an aid in the management of heart, liver, and kidney transplant patients.. Recalled by Siemens Healthcare Diagnostics, Inc.. Units affected: 1586.
Why was this product recalled?
Complaints were received regarding variability in recovery of QC and patient results with certain lots of the Dimension Vista CSA Flex reagent cartridges.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 29, 2014. Severity: Moderate. Recall number: Z-0818-2014.