US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 21, 2012 (14 years ago)

0.9% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, product code…

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

Why it was recalled

Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).

What was recalled

0.9% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E1322, NDC 0338-6304-02; b) 500 mL AVIVA Container, product code 6E1323, NDC 0338-6304-03; Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA

Recalling firm
Baxter Healthcare Corp.
NDC code
0338-6304-02
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1689-2012

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