FDAFDA · Food and drugs·Recall number D-0294-2015
Fentanyl Citrate Injection, USP, 2500 mcg Fentanyl/50 mL, 50 mL Single-dose Flip top Vial (C-II), Rx only, 25 units per box/50 units per case, Hospira Inc., Lake Forest, IL --- NDC 0409-9094-61
Published December 17, 2014 · Recall initiated: December 3, 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; improperly crimped fliptop vials
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FENTANYL CITRATE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot 41-099-DK, exp 01MAY2016, NDC 0409-9094-61
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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