CLASS II Drug recall · Reported 19 Jul 2023 · FDA Enforcement Report

0.9% Sodium Chloride Injection USP Excel Plus Container recalled

B. Braun Medical is recalling 0.9% Sodium Chloride Injection USP Excel Plus Container, distributed nationwide in the US. The recall was initiated on 5 Jul 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 0061858305, 0061858306 Exp 3/31/2025
NDC0264-5802, 0264-5804
Quantity recalled79,880 bags

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-0916-2023
FDA event ID
92640
Recalling firm
B. Braun Medical, Daytona Beach, FL
Manufacturer
B. Braun Medical Inc.
Classification
Class II
Status
Terminated
Recall initiated
5 Jul 2023
FDA classified
13 Jul 2023
Reported
19 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

5 Jul 2023Recall initiated by company
13 Jul 2023Classified by FDA+8 days
19 Jul 2023Published 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: bags have the potential to leak.

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, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA, NDC 0264-5802-00

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Lack of assurance of sterility: bags have the potential to leak.

Which lots are affected?

Lot#: 0061858305, 0061858306 Exp 3/31/2025

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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