Drug recall D-308-2013
Product
Preservative-Free MORPHINE Sulfate Injection, USP, 10 mg/10 mL (1 mg/mL) 10 mL vial, Rx only, HOSPIRA, INC, LAKE FOREST, IL 60045 USA NDC 0409-3815-12
Reason for recall
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial
Lots and codes
Lot 15-065-DK, Exp 1SEP2013
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 26,100 vials
- Distribution
- Nationwide and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 28, 2012
- Terminated
- September 18, 2014
Related products
- Morphine Sulfate – drug information
- NDC 0409-3815 Morphine Sulfate · Morphine Sulfate 1 mg/mL · Hospira, Inc.
- NDC 0409-3814 Morphine Sulfate · Morphine Sulfate .5 mg/mL · Hospira, Inc.