Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay — Class II medical device recall Z-0181-2014
Terminated recall by Siemens Healthcare Diagnostics, Inc., reported 2013-11-13, distributed nationwide. Imprecision with certain lots
| Recall number | Z-0181-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Healthcare Diagnostics, Inc., Newark, DE, United States |
| Recall initiated | 2013-08-30 |
| Classified | 2013-11-07 |
| Reported by FDA | 2013-11-13 |
| Terminated | 2014-08-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | MX |
| Quantity | 4,963 |
| Lot numbers | 1290, 1300, 1313, 1330, 1338, 1367, 1371, 1380, E5-E7, F1-F5 |
Product
Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay
Reason for recall
Imprecision with certain lots
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-0181-2014. 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.