Drug recall D-0490-2015
Product
0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, 60045, NDC: 0409-7101-67
Reason for recall
Lack of Sterility Assurance: The product has the potential to leak at the administrative port.
Lots and codes
Lot# 44-110-JT; Exp 08/16
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 128,050 ADD-Vantage flexible containers
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 7, 2015
- Terminated
- November 4, 2016
Related products
- Sodium Chloride – drug information
- NDC 0409-7101 Sodium Chloride · Sodium Chloride 900 mg/100mL · Hospira, Inc.