PlainRecalls
FDA Drug Moderate Class II Terminated

5% Dextrose Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7922-02

Reported: June 27, 2018 Initiated: May 31, 2018 #D-0885-2018

Product Description

5% Dextrose Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7922-02

Reason for Recall

Lack of assurance of sterility: Bags have potential to leak.

Details

Recalling Firm
ICU Medical Inc
Units Affected
267288 bags
Distribution
Nationwide and Canada
Location
LAKE FOREST, IL

Frequently Asked Questions

What product was recalled?
5% Dextrose Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7922-02. Recalled by ICU Medical Inc. Units affected: 267288 bags.
Why was this product recalled?
Lack of assurance of sterility: Bags have potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 27, 2018. Severity: Moderate. Recall number: D-0885-2018.