Drug recall D-096-2013
Product
Nalbuphine HCl Injection, 20 mg/mL, 10 mL Multiple-dose Fliptop Vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1467-01
Reason for recall
Lack of Assurance of Sterility: Complains of a loose crimp applied to the fliptop vial; and a missing stopper and flip cap were received and therefore sterility cannot be assured.
Lots and codes
Lot #: 11-293-DK, Exp 05/01/13
Recall details
- Recalling firm
- Hospira, Inc., Lake Forest, IL
- Quantity
- 145,400 vials
- Distribution
- Nationwide and Puerto Rico.
- Type
- Voluntary: Firm initiated
- Recall initiated
- November 21, 2012
- Terminated
- June 3, 2014
Related products
- Nalbuphine hydrochloride – drug information
- NDC 0409-1467 Nalbuphine Hydrochloride · Nalbuphine Hydrochloride 20 mg/mL · Hospira, Inc.
- NDC 0409-1463 Nalbuphine Hydrochloride · Nalbuphine Hydrochloride 10 mg/mL · Hospira, Inc.
- NDC 0409-1465 Nalbuphine Hydrochloride · Nalbuphine Hydrochloride 20 mg/mL · Hospira, Inc.
- NDC 0409-1464 Nalbuphine Hydrochloride · Nalbuphine Hydrochloride 10 mg/mL · Hospira, Inc.