FDAFDA · Food and drugs·Recall number D-1232-2015
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
Published July 15, 2015 · Recall initiated: May 19, 2015
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
Failed pH Specifications: 12 month stability testing
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- U.S. Nationwide, Kuwait, Bahrain and Israel.
- Lot
- Lot #: 39-569-DK, Exp 3/1/2016
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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