PHENYLephrine HCl — Class I drug recall D-1826-2015
Terminated recall by Pharmedium Services, LLC, reported 2015-09-30, distributed nationwide. Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injecti
| Recall number | D-1826-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2015-01-28 |
| Classified | 2015-09-23 |
| Reported by FDA | 2015-09-30 |
| Terminated | 2017-01-27 |
| Distributed | Nationwide (US) |
| Quantity | 84 bags |
| Reason classes | specification failure |
| NDC | 61553-0156-50 |
| Lot numbers | 14310063S, 14316086S, 14322138S |
| Expiration dates | 2015-02-04, 2015-02-10, 2015-02-16 |
Product
PHENYLephrine HCl, 20 mg added to 250 mL 0.9% Sodium Chloride Injection USP (80 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-156-50
Reason for recall
Presence of Particulate Matter: The firm manufactured products using Hospira 0.9% Sodium Chloride, USP injection which were subsequently recalled due to the presence of particulate matter (human hair).
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-1826-2015. 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.