FDAFDA · Food and drugs·Recall number D-0153-2017
Fentanyl Citrate Injection, USP, 100 mcg Fentanyl/ 2mL, Single Dose, 50 mcg/mL, Rx only, Hospira, Inc., Lake Forest IL 60045, NDC 0409-4093-32
Published November 30, 2016 · Recall initiated: November 1, 2016
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: Complaints of broken tips on the ampules.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot #5 9277EV, 60028EV, 6008EV, Exp 11/1/17
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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