Class III
Terminated
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.
This recall has been terminated (originally issued June 27, 2012).
- Company
- Hospira Inc.
- Recall Initiated
- April 5, 2012
- Posted
- June 27, 2012
- Recall Number
- D-1390-2012
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 164,568 containers
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Distribution
Nationwide
Lot / Code Info
Lot #: 04510KL*, Exp 01OCT2012; *lot number may have 01 or 02 following it
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