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FDAFDA · Food and drugs·Recall number D-0215-2019

5% Dextrose Injection, USP, Rx Only, a) 25 mL NDC 0409-7923-20; b) 250 mL NDC 0409-7922-02, Hospira, Inc. Lake Forest, IL 60045

Published November 14, 2018 · Recall initiated: October 8, 2018

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of Assurance of Sterility; bags have the potential to leak

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
ICU Medical Inc
Distributor
Nationwide.
Lot
Lots: a) 84-017-JT Exp. December 01, 2019; b) 84-012-JT Exp. June 01, 2019
Risk classification
Class II
Area (FDA)
drug
Country
United States

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