CLASS II Drug recall · Reported 27 Aug 2014 · FDA Enforcement Report

fentaNYL 2500 mcg/ (10 mcg/mL) in 0.9% Sodium Chloride recalled

Healix Infusion Therapy is recalling fentaNYL 2500 mcg/ (10 mcg/mL) in 0.9% Sodium Chloride in flexable, Compounded Drug For, distributed in Georgia, Texas. The recall was initiated on 27 Jun 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots 7230-0, 7269-0 Exp. 08/14
Quantity recalled48 bags

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-1552-2014
FDA event ID
69056
Recalling firm
Healix Infusion Therapy, Sugar Land, TX
Classification
Class II
Status
Terminated
Recall initiated
27 Jun 2014
FDA classified
21 Aug 2014
Reported
27 Aug 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility
Drug class
Pain Medication

Timeline

27 Jun 2014Recall initiated by company
21 Aug 2014Classified by FDA+55 days
27 Aug 2014Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

fentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride in 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 75901-8002-04

Where it was distributed

Texas and Georgia

GeorgiaTexas

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility: Firm received fentanyl from a supplier who recalled it because fliptop vial crimps were loose or missing.

Which lots are affected?

Lots 7230-0, 7269-0 Exp. 08/14

Where was it sold?

Texas and Georgia

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 69056

This product is part of a recall event; the main page for the event is fentaNYL 5000 mcg/ (20 mcg/mL) in 0.9% Sodium Chloride recalled.

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