Drug recall D-0957-2017
Product
0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Distributed in Canada by Baxter Corporation, Toronto, Ontario, Canada, Product Code: 2B1322, NDC 0338-0049-02.
Reason for recall
Lack of Assurance of Sterility: Customer complaints for leaking bags.
Lots and codes
Lot: Y229153, Exp 09/30/18
Recall details
- Recalling firm
- Baxter Healthcare Corporation, Deerfield, IL
- Quantity
- 131,904 bags
- Distribution
- Nationwide in USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 6, 2017
- Terminated
- April 29, 2020
Related products
- Sodium Chloride – drug information
- NDC 0338-0043 Sodium Chloride · Sodium Chloride 4.5 g/1000mL · Baxter Healthcare Corporation
- NDC 0338-0049 Sodium Chloride · Sodium Chloride 9 g/1000mL · Baxter Healthcare Corporation