# FDA recall D-1554-2014

> **Healix Infusion Therapy, Inc.** · Class II · drug recall initiated 2014-06-27.

## Product

fentaNYL 2750 mcg/55 mL (50 mcg/mL) in prefilled syringe, 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  75901-8008-33

## 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.

## Distribution

Texas and Georgia

## Key facts

- **Recall number:** D-1554-2014
- **Recalling firm:** Healix Infusion Therapy, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2014-06-27
- **Report date:** 2014-08-27
- **Termination date:** 2015-08-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sugar Land, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1554-2014

## Citation

> AI Analytics. FDA recall D-1554-2014. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1554-2014. Source: US FDA. Licensed CC0.

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