SIEMENS ADVIA Centaur CP Immunoassay System BNP kit — Class II medical device recall Z-2149-2014
Terminated recall by Siemens Healthcare Diagnostics, Inc, reported 2014-08-13, distributed nationwide. Complaints of failed calibration.
| Recall number | Z-2149-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Healthcare Diagnostics, Inc, East Walpole, MA, United States |
| Recall initiated | 2014-06-23 |
| Classified | 2014-08-05 |
| Reported by FDA | 2014-08-13 |
| Terminated | 2016-03-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BG, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, EE, EG, ES, FI, FR, GB, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JP, KR, LB, LT, LV, MY, NL, NO, OM, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, TH, TR, TW, UA, VE, VN, ZA |
| Quantity | 1,191 kits |
| Lot numbers | 38479172, 39181172 |
Product
SIEMENS ADVIA Centaur CP Immunoassay System BNP kit; SMN 10309044 - 100 test For in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the ADVIA Centaur CP System.
Reason for recall
Complaints of failed calibration.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2149-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.