FDA Drug Recalls

Recalls / Class II

Class IID-1551-2014

Product

fentaNYL 1500 mcg/30 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 75901-8008-90

Affected lot / code info
Lot 7088-0 Exp. 07/14

Why it was recalled

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

Recalling firm

Firm
Healix Infusion Therapy, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1075 W Park One Dr Suite 200, Sugar Land, Texas 77478-2576

Distribution

Quantity
50 syringes
Distribution pattern
Texas and Georgia

Timeline

Recall initiated
2014-06-27
FDA classified
2014-08-21
Posted by FDA
2014-08-27
Terminated
2015-08-25
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1551-2014. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls