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.
Reported: July 19, 2017 Initiated: July 6, 2017 #D-0957-2017
Product Description
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.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 131,904 bags
- Distribution
- Nationwide in USA
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Baxter Healthcare Corporation. Units affected: 131,904 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Customer complaints for leaking bags.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 19, 2017. Severity: Moderate. Recall number: D-0957-2017.
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