RecallDepth
Class II Terminated

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

Company
Hospira Inc., A Pfizer Company
Recall Initiated
May 18, 2017
Posted
June 21, 2017
Recall Number
D-0898-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
(720503A): 43,200 vials, (720603A): 400 vials
Firm Location
Lake Forest, IL, United States

Reason for Recall

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

Distribution

Nationwide, Canada and Singapore

Lot / Code Info

720503A, 720603A (Canada only)

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