Drug recall D-1540-2014
Product
DOBUTamine Injection, USP, 250 mg per 20 mL, 20 mL Single-dose Fliptop Vial, Rx only, Manufactured for Hospira Inc., Lake Forest, IL 60045 USA. NDC 0409-2344-02
Reason for recall
Presence of Particulate Matter: Discolored solution due to a chip in the glass at the neck of the vial, also glass particulate was found within the solution.
Lots and codes
Lot # 27-352-DK; Exp 03/15
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 123,900 vials
- Distribution
- Nationwide and Puerto Rico.
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 10, 2014
- Terminated
- July 14, 2015
Related products
- Dobutamine – drug information
- NDC 0409-2344 Dobutamine · Dobutamine Hydrochloride 12.5 mg/mL · Hospira, Inc.