D-0973-2017 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- July 19, 2017
- Initiation Date
- July 6, 2017
- Termination Date
- April 29, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 295,200 bags
Product Description
0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38
Reason for Recall
Lack of Assurance of Sterility: Bags have the potential to leak.
Distribution Pattern
Nationwide, Puerto Rico and Saudi Arabia
Code Information
Lots: P361501, P361667, and P361790, Exp 09/30/18