FDA Recall 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.

Recall: Z-0818-2014 · Initiated December 5, 2013

Recall

Recall Number
Z-0818-2014
Event Number
67057
Firm
Siemens Healthcare Diagnostics, Inc.
FEI Number
2517506
Product Code
MKW
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
December 5, 2013
Posted
January 23, 2014
Terminated
August 27, 2014
Address
500 Gbc Dr PO BOX 6101, Ms 514, Newark, DE, 19702-2466

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

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

Action

Siegmens sent an Urgent Medical Device Recall lletter dated December 2013 to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discontinue use and discard any remaining inventory of the affected product. Customers were also instructed to complete the attached form and fax it to 302-631-8467. Customers were asked to retain the letter with their laboratory records, and forward the letter to any who have received the affected product. Customers with questions were instructed to contact Siemens Customer Care Center - Technical Solutions or their local Siemens technical support representative. For questions regarding this recall call 800-441-9250.

Distribution

Worldwide Distribution - USA (nationwide) and Canada.

Quantity

1586