Drug recall D-0898-2017

Class II Terminated reported Jun 21, 2017

Product

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

Reason for recall

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

Lots and codes

720503A, 720603A (Canada only)

Recall details

Recalling firm
Hospira Inc., A Pfizer Company, Lake Forest, IL
Quantity
(720503A): 43,200 vials, (720603A): 400 vials
Distribution
Nationwide, Canada and Singapore
Type
Voluntary: Firm initiated
Recall initiated
May 18, 2017
Terminated
May 2, 2019

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