FDAFDA · Food and drugs·Recall number D-169-2013
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Published March 6, 2013 · Recall initiated: January 10, 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; possible loose crimp applied to fliptop vial
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FUROSEMIDE
- Manufacturer
- Hospira, Inc.
- Distributor
- Nationwide
- Lot
- 18-099-DK
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.