US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 2, 2015 (11 years ago)

0.9% Sodium Chloride Injection USP, 50 mL ADD-Vantage Unit, Rx only, Manufactured by…

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

Why it was recalled

Lack of assurance of sterility: Potential channel leaks near the threaded vial port.

What was recalled

0.9% Sodium Chloride Injection USP, 50 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira, Inc., Ausitn, TX 78728, NDC 00409-7101-68

Recalling firm
Hospira Inc.
NDC code
00409-7101-68
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1240-2015

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.

Other Chloride recalls

See all