US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 18, 2017 (9 years ago)

Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only…

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

Why it was recalled

GMP Deviation; A foreign stopper was observed during packaging of a lot of product.

What was recalled

Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04

Recalling firm
Hospira Inc., A Pfizer Company
NDC code
0409-3375-04
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0898-2017

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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