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
Brand: Lactated Ringers
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
Drug class: Injectable & IV Drugs

Timeline

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

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 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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Reported	Class	Recall	Company	Reason	Where
16 Sep 2026Drug	CLASS I	0.9% Sodium Chloride Injection, USP Partial Fill recalledSodium Chloride	B Braun Medical	Particulate Matter	Nationwide
9 Sep 2026Drug	CLASS I	0.9% Sodium Chloride Injection USP, Viaflex recalledSodium Chloride	Baxter Healthcare	Particulate Matter	IL
13 May 2026Drug	CLASS I	Lactated Ringer's Injection USP container recalled by B Braun MedicalLactated Ringers	B Braun Medical	Particulate Matter	Nationwide
29 Apr 2026Drug	CLASS II	Lactated Ringer's Irrigation, Sterile, Ex only recalledLactated Ringers Irrigation	B Braun Medical	Sterility	Nationwide
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