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FDAFDA · Food and drugs·Recall number D-1390-2012

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.

Published June 27, 2012 · Recall initiated: April 5, 2012

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
MAGNESIUM SULFATE IN WATER
Manufacturer
Hospira, Inc.
Distributor
Nationwide
Lot
Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
Risk classification
Class III
Area (FDA)
drug
Country
United States

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