Drug recall D-316-2013
Product
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
Reason for recall
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Lots and codes
Lot 23-320-DK and 23-321-DK Exp. 11/14
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 266,900 vials
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- February 26, 2013
- Terminated
- November 10, 2014
Related products
- Sodium Acetate – drug information
- NDC 0409-7299 Sodium Acetate · Sodium Acetate Anhydrous 3.28 g/20mL · Hospira, Inc.