US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 31, 2018 (8 years ago)

0.9% Sodium Chloride Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

0.9% Sodium Chloride Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7983-02

Recalling firm
ICU Medical Inc
NDC code
0409-7983-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0882-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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