PHENYLephrine added to 0 — Class I drug recall D-0272-2025
Ongoing recall by Central Admixture Pharmacy Services, Inc., reported 2025-03-19, distributed nationwide. Presence of Particulate Matter
| Recall number | D-0272-2025 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Central Admixture Pharmacy Services, Inc., Allentown, PA, United States |
| Recall initiated | 2025-02-20 |
| Classified | 2025-03-11 |
| Reported by FDA | 2025-03-19 |
| Distributed | Nationwide (US) |
| Quantity | 1,546 bags |
| Reason classes | specification failure |
| NDC | 71285-6092-01 |
| Lot numbers | 03MAR2025, 09MAR2025, 10MAR2025, 37-928390, 37-928796, 37-928839 |
| Expiration dates | 2025-03-03, 2025-03-09, 2025-03-10 |
Product
PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.
Reason for recall
Presence of Particulate Matter
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-0272-2025. 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.