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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

B. Braun Lactated Ringer's and Sodium Chloride Injections Recalled for Particles

Agency Publication Date: August 29, 2025
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Summary

B. Braun Medical Inc. is recalling 93,180 containers of Lactated Ringer's Injection USP and 0.9% Sodium Chloride Injection USP because they may contain particulate matter. These products are intravenous (IV) solutions used to replace fluids and electrolytes in patients. The recall affects 46,032 containers of Lactated Ringer's and 47,148 containers of Sodium Chloride distributed nationwide across the United States. If you are a healthcare provider or a facility with these products, you should immediately stop using the affected lots and contact the manufacturer to arrange for their return.

Risk

The presence of particulate matter in an injectable drug can lead to serious health complications, such as inflammation of the veins, blood clots that can travel to the lungs (pulmonary embolism), or other organ damage if the particles enter the bloodstream.

What You Should Do

  1. Identify if you have the affected products by checking the label for Lactated Ringer's Injection USP (NDC 0264-7750-07) or 0.9% Sodium Chloride Injection USP (NDC 0264-7800-09) in 1,000 mL containers.
  2. Check the specific lot numbers and expiration dates: for Lactated Ringer's, look for lot J4S807 with an expiration date of 5/31/2027; for Sodium Chloride, look for lot V3K770 with an expiration date of 1/31/2026.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

📋Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Lactated Ringer's Injection USP (1000 mL)
Variants: Rx only
Lot Numbers:
J4S807 (Exp 5/31/2027)
NDC:
0264-7750-07

Recall #: D-0627-2025; Quantity: 46,032 containers

Product: 0.9% Sodium Chloride Injection USP (1000 mL)
Variants: Rx only
Lot Numbers:
V3K770 (Exp 1/31/2026)
NDC:
0264-7800-09

Recall #: D-0628-2025; Quantity: 47,148 containers

Product Images

1: 0.9% Sodium Chloride Injection USP 1000 mL

1: 0.9% Sodium Chloride Injection USP 1000 mL

Lactated Ringer’s Injection USP 1000 mL

Lactated Ringer’s Injection USP 1000 mL

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97433
Status: Active
Manufacturer: B BRAUN MEDICAL INC
Sold By: wholesalers; hospitals; medical distributors
Manufactured In: United States
Units Affected: 2 products (46,032 containers; 47,148 containers)
Distributed To: Nationwide
Agency Last Updated: September 10, 2025

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.