CLASS II Drug recall · Reported 14 Dec 2022 · FDA Enforcement Report

0.9% Sodium Chloride Injection USP Single-dose container recalled

B. Braun Medical is recalling 0.9% Sodium Chloride Injection USP Single-dose container, distributed in Florida, New Jersey, Pennsylvania. The recall was initiated on 25 Nov 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 0061832446 Exp. 31 Oct 2024
NDC0264-5802, 0264-5804
Quantity recalled756 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-0076-2023
FDA event ID
91194
Recalling firm
B. Braun Medical, Allentown, PA
Manufacturer
B. Braun Medical Inc.
Classification
Class II
Status
Terminated
Recall initiated
25 Nov 2022
FDA classified
5 Dec 2022
Reported
14 Dec 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

25 Nov 2022Recall initiated by company
5 Dec 2022Classified by FDA+10 days
14 Dec 2022Published in enforcement report+9 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 sterility assurance: 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 Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA 1-800-227-2862

Where it was distributed

FL, NJ, PA

FloridaNew JerseyPennsylvania

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot: 0061832446 Exp. 31 Oct 2024

Where was it sold?

FL, NJ, PA

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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