CLASS I ONGOING Drug recall · Reported 2 Sep 2026 · FDA Enforcement Report

Lactated Ringer's Injection USP Excel container recalled

B Braun Medical is recalling Lactated Ringer's Injection USP Excel container, distributed nationwide in the US. The recall was initiated on 12 Aug 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot#: J4H077, Exp 30NOV2026.
NDC0264-7750
Quantity recalled23,688 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-0832-2026
FDA event ID
99633
Recalling firm
B Braun Medical, Allentown, PA
Manufacturer
B. Braun Medical Inc.
Classification
Class I
Status
Ongoing
Recall initiated
12 Aug 2026
FDA classified
3 Sep 2026
Reported
2 Sep 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Particulate Matter

Timeline

12 Aug 2026Recall initiated by company
2 Sep 2026Published in enforcement report+21 days
3 Sep 2026Classified by FDA+1 day

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

Reason for recall

Presence of Particulate matter.

Product as listed by the FDA

Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00

Where it was distributed

U.S. Nationwide

Nationwide

Questions about this recall

Is Lactated Ringer's Injection USP Excel container recalled?

Yes. B Braun Medical recalled Lactated Ringer's Injection USP Excel container on 12 Aug 2026. The recall is Class I and its status is Ongoing. Recall number D-0832-2026.

Why was it recalled?

Presence of Particulate matter.

Which lots are affected?

Lot#: J4H077, Exp 30NOV2026.

Where was it sold?

U.S. 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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 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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