Pentreotide — Class II drug recall D-1399-2019
Terminated recall by Synthetopes Inc, reported 2019-06-19, distributed nationwide. Lack of Processing Controls.
| Recall number | D-1399-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthetopes Inc, Conway, SC, United States |
| Recall initiated | 2019-05-28 |
| Classified | 2019-06-20 |
| Reported by FDA | 2019-06-19 |
| Terminated | 2020-10-15 |
| Distributed | Nationwide (US) |
| Quantity | 20 vials |
Product
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Reason for recall
Lack of Processing Controls.
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-1399-2019. 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.