FDAFDA · Food and drugs·Recall number D-1433-201
Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, C-II, (50 mcg/mL), 50 mL Single-dose Fliptop Vial, Rx only. Hospira, Inc., Lake Forest, IL 60045. NDC: 0409-9094-61.
Published July 23, 2014 · Recall initiated: June 27, 2014
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: Fliptop vial crimps are loose or missing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FENTANYL CITRATE
- Manufacturer
- Hospira Inc.
- Distributor
- U.S. Nationwide
- Lot
- Lot #: 39474DK, Expiry: 03/01/2016.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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