Recall Z-0343-2011

Siemens Healthcare Diagnostics, Inc. · initiated December 7, 2009

Terminated

Product

Stratus(R) CS Rotors, catalog number CROTOR, lot number NH42-251-09 Intended use: Stratus(R) rotors is intended for the separation of whole blood samples for analysis on the Stratus(R) CS analyzer

Codes / lots: catalog number CROTOR, lot number NH42-251-09

Reason for recall

Low frequency defect in the gel filling of this lot that may result in inadequate separation of cells in centrifugation.

FDA-determined cause: Process control

Action taken

The recalling firm, SIEMENS, issued an "Urgent Field Safety Notice" dated December 2009 to all affected customers. The notice described the product, problem and the action to be taken by the customers. The customers were instructed to review the situation with their laboratory director to determine the need to evaluate previously reported test results; immediately examine their CROTOR inventory and discard all bags that are from lot NH42-251-09 including rotors that were not stored in their original packaging (bag); contact Siemens Customer Service Center at 800-241-0420 to request additional no-charge replacements (Note: A "no-charge" order has already been placed so that one bag of replacement rotors would be recieved shortly); forward this notice to anyone they may have distributed this product, and complete and return the FIELD CORRECTION EFFECTIVENESS CHECK via fax at 302-631-8467. If you have any questions regarding this information, please contact the Siemens Technical Solution Center at 800-405-6473.

Details

Recall number
Z-0343-2011
Initiated
December 7, 2009
Posted by FDA
November 10, 2010
Terminated
November 10, 2010
Product code
JHX – Fluorometric Method, Cpk Or Isoenzymes
Quantity
330 bags
Distribution
Worldwide distribution: USA including states of AK, AZ, AR, CA, FL, GA, HI, IA, IL, IN, KY, LA, MI, MN, MO, MS, MT, NC, ND, NH, NM, NY, OH, TX, UT, WA, WI, and WV and country of Canada
Recalling firm
Siemens Healthcare Diagnostics, Inc., Newark, DE

Official FDA recall record