Drug recall D-613-2013
Product
0.45% Sodium Chloride Injection, USP, Rx Only, 250 mL, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7132-02
Reason for recall
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Lots and codes
Lot #: 93-153-JT, Exp 9/12
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 136,584 units
- Distribution
- Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 4, 2012
- Terminated
- July 17, 2015
Related products
- Sodium Chloride – drug information
- NDC 0409-7101 Sodium Chloride · Sodium Chloride 900 mg/100mL · Hospira, Inc.