Drug recall D-0294-2015
Product
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
Reason for recall
Lack of Assurance of Sterility; improperly crimped fliptop vials
Lots and codes
Lot 41-099-DK, exp 01MAY2016, NDC 0409-9094-61
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 62,650 vials
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 3, 2014
- Terminated
- October 2, 2015
Related products
- Fentanyl Citrate – drug information
- NDC 0409-9093 Fentanyl Citrate · Fentanyl Citrate 50 ug/mL · Hospira, Inc.
- NDC 0409-9094 Fentanyl Citrate · Fentanyl Citrate 50 ug/mL · Hospira, Inc.