Hospira Inc. recalls Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospi
Recalled July 15, 2015 · FDA recall D-1232-2015 · Hospira
Hazard
Failed pH Specifications: 12 month stability testing · FDA Class III
Units
106,900 vials
Sold at
U.S. Nationwide, Kuwait, Bahrain and Israel.
Description
Failed pH Specifications: 12 month stability testing
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
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →