ADVIA Centaur Vitamin D Assay — Class II medical device recall Z-1120-2013
Terminated recall by Siemens Healthcare Diagnostics, Inc, reported 2013-04-24, distributed nationwide. Negative bias in patient samples for Vitamin D
| Recall number | Z-1120-2013 |
|---|---|
| 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 | 2013-03-13 |
| Classified | 2013-04-15 |
| Reported by FDA | 2013-04-24 |
| Terminated | 2015-03-05 |
| Distributed | Nationwide (US) |
| Quantity | 4,133 |
| Lot numbers | 134009, 134010, 134011, 88767009, 88787009, 90253010, 91934010, 92396011, 93363011, 95088011 |
Product
ADVIA Centaur Vitamin D Assay (500 tests); Reference Number:10631021. For use in the quantitative determination of Vit D.
Reason for recall
Negative bias in patient samples for Vitamin D
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-1120-2013. 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.