Recall Z-0541-2014

Siemens Healthcare Diagnostics, Inc. · initiated September 18, 2013

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Siemens Dimension Vista Homocysteine Flex Reagent Cartridge The HCYS method is an in vitro diagnostic test for the quantitative measurement of total homocysteine in human serum, heparinized plasma and ETDA plasma on the Dimension Vista System. Measurements of homocysteine aid in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria.

Codes / lots: lot 13064MA, expiration 2014-03-05

Reason for recall

Dimension Vista HCYS lot 13064MA shows erratic recovery of QC and patient samples.

FDA-determined cause: Unknown/Undetermined by firm

Action taken

Siemens sent a Urgent Medical Device Recall letter dated September 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customers. Actions to be taken by Customer: Please discontinue use and discard any remaining inventory of Dimension Vista HCYS Flex reagent cartridge (Catalog# K7044) lot 13064MA. Please complete the attached form and fax it to (302) 631-8467 to facilitate your no charge replacement needs. Please retain this letter with your laboratory records, and forward this letter to those who may have received this product. We apologize for the inconvenience this situation has caused. If you have any questions, please contact your Siemens Customer Care Center- Technical Solutions or your local Siemens technical support representative. For further questions please call (800) 441-9250.

Details

Recall number
Z-0541-2014
Initiated
September 18, 2013
Posted by FDA
December 19, 2013
Terminated
October 1, 2014
Product code
LPS – Urinary Homocystine (Nonquantitative) Test System
Quantity
302
Distribution
Worldwide Distribution - US Distribution including the states of OH, MD, CO, NJ, IA, NC, VA, WI and DC., and the countries of Austria, Denmark, France, Italy, Netherlands and Norway.
Recalling firm
Siemens Healthcare Diagnostics, Inc., Newark, DE

Official FDA recall record