Drug recall D-1390-2012
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.
Reason for recall
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Lots and codes
Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
Recall details
- Recalling firm
- Hospira, Inc., Lake Forest, IL
- Quantity
- 164,568 containers
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 5, 2012
- Terminated
- August 8, 2013
Related products
- Magnesium Sulfate in Water – drug information
- NDC 0409-5239 Magnesium Sulfate in Water · Magnesium Sulfate Heptahydrate 2 g/50mL · Hospira, Inc.
- NDC 0409-3164 Magnesium Sulfate in Water · Magnesium Sulfate Heptahydrate 40 g/1000mL · Hospira, Inc.
- NDC 0409-6729 Magnesium Sulfate in Water · Magnesium Sulfate Heptahydrate 40 mg/mL · Hospira, Inc.
- NDC 0409-2050 Magnesium Sulfate in Water · Magnesium Sulfate Heptahydrate 20 g/500mL · Hospira, Inc.
- NDC 0409-4121 Magnesium Sulfate in Water · Magnesium Sulfate Heptahydrate 4 g/100mL · Hospira, Inc.