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.
Reported: June 27, 2012 Initiated: April 5, 2012 #D-1390-2012
Product Description
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.
Details
- Recalling Firm
- Hospira, Inc.
- Units Affected
- 164,568 containers
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Hospira, Inc.. Units affected: 164,568 containers.
Why was this product recalled? ▼
Superpotent (Single Ingredient) Drug: Above specification assay results for percentage of magnesium sulfate.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 27, 2012. Severity: Low. Recall number: D-1390-2012.
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