5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B0089, NDC: 0338-0017-38
Reported: July 19, 2017 Initiated: July 6, 2017 #D-0972-2017
Product Description
5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B0089, NDC: 0338-0017-38
Reason for Recall
Lack of Assurance of Sterility: Bags have the potential to leak.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 54,528 bags
- Distribution
- Nationwide, Puerto Rico and Saudi Arabia
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
5% Dextrose Injection, USP, 100 mL VIAFLEX Plastic Container, Rx only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B0089, NDC: 0338-0017-38. Recalled by Baxter Healthcare Corporation. Units affected: 54,528 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Bags have the potential to leak.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 19, 2017. Severity: Moderate. Recall number: D-0972-2017.
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