CLASS II ONGOING Drug recall · Reported 20 Aug 2025 · FDA Enforcement Report

0.9% Sodium Chloride Injection USP, L 8000 Excel Container recalled

B Braun Medical is recalling 0.9% Sodium Chloride Injection USP, L 8000 Excel Container, distributed nationwide in the US. The recall was initiated on 4 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: J5C919, Exp. 08/31/2027
NDC0264-7800, 0264-7802
Quantity recalled23,100 containers

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0586-2025
FDA event ID
97368
Recalling firm
B Braun Medical, Allentown, PA
Manufacturer
B. Braun Medical Inc.
Classification
Class II
Status
Ongoing
Recall initiated
4 Aug 2025
FDA classified
14 Aug 2025
Reported
20 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

4 Aug 2025Recall initiated by company
14 Aug 2025Classified by FDA+10 days
20 Aug 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

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.

Where it was distributed

Nationwide in the US

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot #: J5C919, Exp. 08/31/2027

Where was it sold?

Nationwide in the US

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 97368
ReportedClassRecallCompanyReasonWhere
CLASS IILactated Ringer's Injection USP, L 7500 Excel Container recalledLactated RingersB Braun MedicalSterilityNationwide

More recalls from B Braun Medical

All 447

Other Sodium Chloride recalls

All 133