US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 4, 2025 (13 months ago)

0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container, Rx Only, Sterile…

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

Why it was recalled

Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.

What was recalled

0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7800-00.

Recalling firm
B Braun Medical INC
NDC code
0264-7800-00
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0586-2025

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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