FDAFDA · Food and drugs·Recall number D-316-2013
Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-7299-73
Published May 15, 2013 · Recall initiated: February 26, 2013
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
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM ACETATE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot 23-320-DK and 23-321-DK Exp. 11/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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