Drug recall D-1232-2015

Class III Terminated reported Jul 15, 2015

Product

Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd Rocky Mount, NC 27804 for Hospira, Inc. 275 N Field Drive, Lake Forest, IL 60045. NDC 0409-2168-02

Reason for recall

Failed pH Specifications: 12 month stability testing

Lots and codes

Lot #: 39-569-DK, Exp 3/1/2016

Recall details

Recalling firm
Hospira Inc., Lake Forest, IL
Quantity
106,900 vials
Distribution
U.S. Nationwide, Kuwait, Bahrain and Israel.
Type
Voluntary: Firm initiated
Recall initiated
May 19, 2015
Terminated
December 4, 2017

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