US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 8, 2013 (14 years ago)

0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC…

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

Why it was recalled

Lack of Assurance of Sterility: There is the potential for solution to leak from the administrative port to the fill tube seal.

What was recalled

0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,

Recalling firm
Hospira Inc.
NDC code
0409-7984-23
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-183-2013

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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