RecallDepth
Class II Terminated

Levophed (norepinephrine bitartrate) injection, USP, 4 mg/4 mL (1mg/mL), 4mL Fill in 5 mL Single dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3375-04

Company
Pfizer Inc.
Recall Initiated
August 22, 2017
Posted
September 27, 2017
Recall Number
D-1168-2017
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
98,050 vials
Firm Location
New York, NY, United States

Reason for Recall

Lack of sterility assurance: resulting from use of a damaged sterilizing filter for nitrogen used in the manufacturing process.

Distribution

United States Nationwide (including Puerto Rico) and Singapore

Lot / Code Info

Lot #: 753003A, Exp 9/18; 762153A, 760803A, 761053A , Exp 10/18

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