CLASS II ONGOING Drug recall · Reported 2 Jul 2025 · FDA Enforcement Report

0.9% Sodium Chloride Injection recalled by B Braun Medical

B Braun Medical is recalling 0.9% Sodium Chloride Injection USP, distributed nationwide in the US. The recall was initiated on 16 Jun 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: J4L260, J4L261, J4L270, J4L271, J4L280, Exp 2/28/2027
NDC0264-7800, 0264-7802
Quantity recalled187,656 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-0491-2025
FDA event ID
97059
Recalling firm
B Braun Medical, Allentown, PA
Manufacturer
B. Braun Medical Inc.
Classification
Class II
Status
Ongoing
Recall initiated
16 Jun 2025
FDA classified
24 Jun 2025
Reported
2 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

16 Jun 2025Recall initiated by company
24 Jun 2025Classified by FDA+8 days
2 Jul 2025Published in enforcement report+8 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: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.

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, 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.

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot #: J4L260, J4L261, J4L270, J4L271, J4L280, Exp 2/28/2027

Where was it sold?

USA Nationwide

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.

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