Drug recall D-1036-2014
Product
Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.
Reason for recall
Lack of Assurance of Sterility; potential leakage from administrative port.
Lots and codes
Lot #: 26-125-JT, Exp: 8/14
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 27780 bags
- Distribution
- Nationwide including Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 9, 2014
- Terminated
- May 19, 2015
Related products
- Heparin Sodium – drug information
- NDC 0409-1005 Heparin Sodium · Heparin Sodium 200 [USP'U]/100mL · Hospira, Inc.
- NDC 0409-2222 Heparin Sodium · Heparin Sodium 200 [USP'U]/100mL · Hospira, Inc.