ClearanceBrief
Recall Z-0113-2019 ยท JHS Differential Rate Kinetic Method, Cpk Or Isoenzymes

Siemens Healthcare Diagnostics, Inc

ADVIA Centaur CKMB Calibrator, Cat No. 09318028 Product Usage: For in vitro diagnostic use in calibrating ADVIA Centaur systems CKMB assays.

DateJul 24, 2018
StatusTerminated
ReasonA potential bias was identified with certain kits compared to the internal standards.
Root causeNonconforming Material/Component
ActionOn July 24, 2018 Siemens Healthineers issued Urgent Medical Device Recall notices to U.S. customers and Urgent Field Safety Notices to OUS customers. The following are Actions to be Taken by the Customer: Customers using ADVIA Centaur CKMB Calibrator Lots ending in 64: - Review the notice with your Medical Director. - Review your inventory of these products and immediately order replacement ADVIA Centaur CKMB Calibrator kit lots ending in 68 by completing the Field Correction Effectiveness Check Form attached to the letter. - You may continue use of ADVIA Centaur CKMB Calibrator kit lots u
Quantity1870 kits
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K962126ACS CKMB II IMMUNOASSAY
Ciba Corning Diagnostics Corp., Jun 21, 1996