ADVIA Centaur Intact PTH Calibrator — Class III medical device recall Z-0173-2014
Terminated recall by Siemens Healthcare Diagnostics, Inc, reported 2013-11-13, distributed nationwide. PTH Calibrator packaged with only high calibrator.
| Recall number | Z-0173-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Healthcare Diagnostics, Inc, East Walpole, MA, United States |
| Recall initiated | 2013-08-16 |
| Classified | 2013-11-06 |
| Reported by FDA | 2013-11-13 |
| Terminated | 2014-02-13 |
| Distributed | Nationwide (US) |
| Lot numbers | 14136A16 |
| Model numbers | 10492387 |
Product
ADVIA Centaur Intact PTH Calibrator (6 pack); Catalog Number: SMN 10492387 For in vitro diagnostic use in calibrating Intact PTH assays on the ADVIA Centaur Systems.
Reason for recall
PTH Calibrator packaged with only high calibrator.
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-0173-2014. 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.