Dextrose Injection,USP,70% 2000 mL VIAFLEX Plastic Container Bag, Pharmacy Bulk Package, Not For ...

FDA Recall #D-0958-2016 — Class I — December 15, 2015

Recall #D-0958-2016 Date: December 15, 2015 Classification: Class I Status: Terminated

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.

Recalling Firm

Baxter Healthcare Corp. — Deerfield, IL

Classification

Class I — Reasonable probability of serious adverse health consequences or death.

Product Type

Drugs

Product Quantity

28,080 VIAFLEX Plastic Containers

Distribution

Nationwide

Code Information

Lot # C985150; Exp. 07/16

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated