Early TPN — Class II drug recall D-0805-2017
Terminated recall by Advanced Pharma Inc., reported 2017-05-31, distributed nationwide. Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
| Recall number | D-0805-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Pharma Inc., Houston, TX, United States |
| Recall initiated | 2017-02-22 |
| Classified | 2017-05-23 |
| Reported by FDA | 2017-05-31 |
| Terminated | 2017-10-18 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
Product
Early TPN (Neonatal) all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Reason for recall
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
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/D-0805-2017. 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.