Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd Rocky Mount, NC 27804 for Hospira, Inc. 275 N Field Drive, Lake Forest, IL 60045. NDC 0409-2168-02
Reported: July 15, 2015 Initiated: May 19, 2015 #D-1232-2015
Product Description
Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd Rocky Mount, NC 27804 for Hospira, Inc. 275 N Field Drive, Lake Forest, IL 60045. NDC 0409-2168-02
Reason for Recall
Failed pH Specifications: 12 month stability testing
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 106,900 vials
- Distribution
- U.S. Nationwide, Kuwait, Bahrain and Israel.
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Magnesium Sulfate Injection, USP, 50%, 20mL, Single dose Fliptop Vial, For IV or IM use, Rx only, Manufactured by Hospira, Inc. 4285 Wesleyan Blvd Rocky Mount, NC 27804 for Hospira, Inc. 275 N Field Drive, Lake Forest, IL 60045. NDC 0409-2168-02. Recalled by Hospira Inc.. Units affected: 106,900 vials.
Why was this product recalled? ▼
Failed pH Specifications: 12 month stability testing
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 15, 2015. Severity: Low. Recall number: D-1232-2015.
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