Drug recall D-169-2013
Product
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Reason for recall
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Lots and codes
18-099-DK
Recall details
- Recalling firm
- Hospira, Inc., Rocky Mount, NC
- Quantity
- 63,900 vials
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 10, 2013
- Terminated
- October 8, 2014
Related products
- Furosemide – drug information
- NDC 0409-6102 Furosemide · Furosemide 10 mg/mL · Hospira, Inc.