Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0719-06
Reported: June 15, 2016 Initiated: December 15, 2015 #D-0958-2016
Product Description
Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0719-06
Reason for Recall
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Details
- Recalling Firm
- Baxter Healthcare Corp.
- Units Affected
- 28,080 VIAFLEX Plastic Containers
- Distribution
- Nationwide
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For Direct Infusion, Must Be Diluted, Rx Only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, NDC 0338-0719-06. Recalled by Baxter Healthcare Corp.. Units affected: 28,080 VIAFLEX Plastic Containers.
Why was this product recalled? ▼
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 15, 2016. Severity: Critical. Recall number: D-0958-2016.
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