US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 16, 2025 (15 months ago)

0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and…

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

Why it was recalled

Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

What was recalled

0.9% Sodium Chloride Injection USP, 500 mL, packaged in 500 mL excel containers and further packaged 24 per case, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018-3524, USA, NDC 0264-7800-10.

Recalling firm
B Braun Medical INC
NDC code
0264-7800-10
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0491-2025

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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