Hospira, Inc. recalls Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only, Ho
Recalled June 27, 2012 · FDA recall D-1390-2012 · Hospira
Hazard
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate. · FDA Class III
Units
164,568 containers
Sold at
Nationwide
Description
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Product
Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, Rx only, Hospira, Inc., Lake Forest, IL 60045; NDC 0409-6729-24.
Manufacturer(s)
Hospira, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →