Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing… — Class II medical device recall Z-1927-2014
Terminated recall by Siemens Healthcare Diagnostics, Inc, reported 2014-07-02, distributed nationwide. Swollen acid bottles due to a trace metal contamination in the Acid Reagent bottles
| Recall number | Z-1927-2014 |
|---|---|
| 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 | 2014-06-02 |
| Classified | 2014-06-26 |
| Reported by FDA | 2014-07-02 |
| Terminated | 2015-02-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, CA, CN, CO, GT, KR, MX, NZ, SG |
| Quantity | 3,839 kits |
| Lot numbers | 454778, 454779 |
| Model numbers | 10310026, 112219 |
| Expiration dates | 2015-02-28 |
Product
Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing ADVIA Centaur Acid Reagent bottles, lot number: 454778 Kit Catalog Number: 112219 SMN: 10310026 Intended Use: In vitro diagnostic use. Acid Regent is a component of the ADVIA Centaur and ADVIA Centaur XP instruments
Reason for recall
Swollen acid bottles due to a trace metal contamination in the Acid Reagent bottles
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-1927-2014. 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.