PHENYLephrine in 0 — Class II drug recall D-0006-2024
Terminated recall by Central Admixture Pharmacy Services Inc, reported 2023-10-11, distributed nationwide. Lack of assurance of sterility:
| Recall number | D-0006-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Central Admixture Pharmacy Services Inc, San Diego, CA, United States |
| Recall initiated | 2023-09-21 |
| Classified | 2023-10-04 |
| Reported by FDA | 2023-10-11 |
| Terminated | 2025-03-19 |
| Distributed | Nationwide (US) |
| Quantity | 3,081 syringes |
| Reason classes | sterility |
| NDC | 71286-6008-01 |
| Lot numbers | 17-275323, 17-275345, 17-275642, 17-275643, 17-275671, 17-275675, 17-275677, 17-276188 |
| Expiration dates | 2023-10-03, 2023-10-08, 2023-10-09, 2023-10-18 |
Product
PHENYLephrine in 0.9 sodium chloride, 800 mcg/10 mL, (80 mcg/mL), 10 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-6008-1
Reason for recall
Lack of assurance of sterility:
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-0006-2024. 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.