Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Mar 22, 2024 (3 years ago)

Lactated Ringer's Injection USP

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Cause type: Sterility / contamination

A product that must be sterile could not be assured sterile, or was contaminated. A top reason for injectables, eye drops and IV products - loss of sterility assurance can lead to serious infections. All sterility / contamination recalls.

What was recalled

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

Affected NDC 0264-7750-00

Compare with the code on your package — it is the most precise check available.

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Lactated Ringers
Sodium Chloride, Sodium Lactate, Potassium Chloride, and Calcium Chloride
NDC 00264-7750
SODIUM CHLORIDE .6 g/100mL; SODIUM LACTATE .31 g/100mL; POTASSIUM CHLORIDE .03 g/100mL; CALCIUM CHLORIDE .02 g/100mL Injection, Solution
Intravenous
B. Braun Medical Inc. Rx
Recalling firm
B. Braun Medical Inc
NDC code
0264-7750-00
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0431-2024 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by B. Braun Medical Inc

All 2024 recalls

Other sterility / contamination recalls from 2024

All sterility / contamination recalls
Class II · Moderate risk

ketamine inj 50 mg per 1 mL

Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.

Terminated Sterility / contamination Hikma Injectables USA Inc NDC 63037-137-25 D-0173-2025