Drug recall D-1424-2014
Product
Labetalol Hydrochloride Injection, USP, 100 mg/20 mL (5 mg/mL), 20 mL Multidose Vial, packaged 50/20 mL glass vials/carton, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-2267-20
Reason for recall
Presence of Particulate Matter; metal embedded in the glass vial and visible particles floating in the solution
Lots and codes
Lot 36225DD, exp 12/01/2015
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 45,448 vials
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 16, 2014
- Terminated
- March 16, 2017
Related products
- Labetalol Hydrochloride – drug information
- NDC 0409-0125 Labetalol Hydrochloride · Labetalol Hydrochloride 5 mg/mL · Hospira, Inc.