0.9% Sodium Chloride Injection USP, 100 mL Viaflex Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0049-38.
Reported: July 31, 2019 Initiated: July 18, 2019 #D-1514-2019
Product Description
0.9% Sodium Chloride Injection USP, 100 mL Viaflex Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0049-38.
Reason for Recall
Lack of Assurance of Sterility: Bags have potential to leak.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 139,680 Containers
- Distribution
- Nationwide in the United States and Puerto Rico.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
0.9% Sodium Chloride Injection USP, 100 mL Viaflex Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0049-38.. Recalled by Baxter Healthcare Corporation. Units affected: 139,680 Containers.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Bags have potential to leak.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 31, 2019. Severity: Moderate. Recall number: D-1514-2019.
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