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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