ADVIA Centaur Systems Insulin ReadyPack; Test Code: IRI; Catalog Number: 02230141, for in vitro diagnostic use in the quantitative determination of insulin in serum.
Recall
- Recall Number
- Z-2086-2017
- Event Number
- 76992
- Firm
- Siemens Healthcare Diagnostics, Inc
- FEI Number
- 1219913
- Product Code
- CFP
- Status
- Terminated
- Root Cause
- Nonconforming Material/Component
- Initiated
- April 5, 2017
- Posted
- April 19, 2017
- Terminated
- April 2, 2019
- Address
- 333 Coney St, East Walpole, MA, 02032-1516
Description
ADVIA Centaur Systems Insulin ReadyPack; Test Code: IRI; Catalog Number: 02230141, for in vitro diagnostic use in the quantitative determination of insulin in serum.
Current lots of ADVIA Centaur/XP/XPT/CP Insulin (IRI) assay recover approximately 40% higher than the World Health Organization (WHO) 1st IRP 66/304 standardization based on slope values. Other performance characteristics are being met per the assay Instructions for Use. Overall risk to health is negligible and Siemens is not recommending a review of previously generated results.
Siemens issued a UMDC to ADVIA Centaur/XP/XPT/CP IRI customers on April 5, 2017. They were informed of the issue & that they may continue use of current product but should discontinue when corrected product is available (reagent lots ending in 201 with cal lots ending in 02). A shift down will occur with the corrected product. BioRad control ranges will be posted to QCnet.com for the corrected reagents.
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