US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 20, 2016 (10 years ago)

Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride 250 mL bag, Rx Only, Compounded by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

What was recalled

Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride 250 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0189-02

Recalling firm
Pharmakon Pharmaceuticals, Inc.
NDC code
45183-0189-02
Origin
IN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1277-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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