FDA Drug Recalls

Recalls / Active ingredient / Magnesium Sulfate Heptahydrate

Magnesium Sulfate Heptahydrate

5 FDA drug recalls involving the active ingredient “Magnesium Sulfate Heptahydrate” — 2 Class I.

DateClassProductFirm
2018-10-03Class IIMagnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose ContainePfizer Inc.
2016-01-05Class IMagnesium Sulfate in Water for Injection, (0.325 mEq Mg++/mL) 40 mg/mL, 2 g Total, 50 mL Single-Dose ContainerHospira Inc.
2015-04-28Class IIKABIVEN [(3.9%) Lipid Injectable Emulsion with (3.1%) Amino Acids and Electrolytes and (9.8%) Dextrose; SulfitFresenius Kabi USA, LLC
2015-03-06Class IMAGNESIUM SULFATE IN 5% DEXTROSE INJECTION, USP, 10 mg/mL; 100 mL bag, Rx only, Hospira, Inc., Lake Forest, ILHospira Inc.
2012-04-05Class IIIMagnesium Sulfate in Water for Injection, 40 mg/mL (0.325 mEq Mg++/mL), 2 g total, 50 mL Flexible Container, RHospira, Inc.