fentaNYL 5000 mcg/250 mL — Class II drug recall D-1555-2014
Terminated recall by Healix Infusion Therapy, Inc., reported 2014-08-27, distributed in GA, TX. Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial cr
| Recall number | D-1555-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Healix Infusion Therapy, Inc., Sugar Land, TX, United States |
| Recall initiated | 2014-06-27 |
| Classified | 2014-08-21 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2015-08-25 |
| Distributed | GA, TX |
| Reason classes | sterility |
| NDC | 75901-8015-04 |
| Lot numbers | 08/14, 7257-0 |
Product
fentaNYL 5000 mcg/250 mL (20 mcg/mL) in 0.9% Sodium Chloride in a flexable bag, COMPOUNDED DRUG For Institutional or Office Use Only--Not for Resale, Federal Law Prohibits Dispensing without Prescription Healix Infusion Therapy, Inc. (866) 298-4826 1075 West Park One Drive, Suite 200, Sugar Land, Texas, 77478, NDC 75901-8015-04
Reason for recall
Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.
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-1555-2014. 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.