Drug recall D-314-2013
Product
Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-6102-04
Reason for recall
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Lots and codes
Lot 20-564-DK Exp. 02/14
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 259,050 vials
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- February 26, 2013
- Terminated
- November 10, 2014
Related products
- Furosemide – drug information
- NDC 0409-6102 Furosemide · Furosemide 10 mg/mL · Hospira, Inc.