Hospira, Inc. recalls Magnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mE
Recalled 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.
Hazard / Issue
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
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