PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: November 14, 2018 Initiated: October 8, 2018 #D-0215-2019

Product Description

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

Reason for Recall

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

Details

Recalling Firm
ICU Medical Inc
Units Affected
372,912 bags
Distribution
Nationwide.
Location
LAKE FOREST, IL

Frequently Asked Questions

What product was recalled?
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. Recalled by ICU Medical Inc. Units affected: 372,912 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 November 14, 2018. Severity: Moderate. Recall number: D-0215-2019.