C-PAV/PHENTOL/PGE1 — Class II drug recall D-0208-2017
Terminated recall by Colonia Care Pharmacy, reported 2016-12-28, distributed in NJ, NY. Lack of Assurance of Sterility; sterility concerns with all injectable drug products that were made with steri
| Recall number | D-0208-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Colonia Care Pharmacy, Colonia, NJ, United States |
| Recall initiated | 2016-07-28 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2023-12-06 |
| Distributed | NJ, NY |
| Reason classes | sterility |
| Expiration dates | 2016-05-22 |
Product
C-PAV/PHENTOL/PGE1, All strengths, All sizes, Rx only, Colonia Care Pharmacy, Colonia NJ 07067
Reason for recall
Lack of Assurance of Sterility; sterility concerns with all injectable drug products that were made with sterilized filtered stock solutions.
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-0208-2017. 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.