Recall Summary
| Recall number | D-0832-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-09-02 |
| Company | B BRAUN MEDICAL INC |
| Units affected | 23,688 |
| Severity | Class I |
Remedy: Follow the instructions in the official notice linked below. The agency record for this recall did not contain remedy text we could verify against this product, so we have not reproduced it here.
Read the official U.S. Food and Drug Administration recall notice
braun medical recall notices matter most when the product goes straight into a vein. On September 2, 2026, the U.S. Food and Drug Administration listed a Class I recall involving B. Braun Medical Inc. The product is Lactated Ringer’s Injection USP, 1000 mL, in the EXCEL container.
The recall number is D-0832-2026. The stated hazard is the presence of particulate matter. Class I is the FDA’s most serious category. It is used when the agency believes exposure could cause serious harm or death. This guide explains what the recall covers and what to do next.
What the Braun Medical Recall Covers
The braun medical recall applies to a single intravenous solution product. The agency record identifies it as Lactated Ringer’s Injection USP, 1000 mL EXCEL container. It is a prescription-only product. The product code is listed as L7500. The NDC number is 0264-7750-00. The listed manufacturer address is B. Braun Medical, Inc., Bethlehem, PA 18018-3524, USA.
Lactated Ringer’s solution is a common IV fluid. Hospitals use it for fluid replacement and volume support. For example, it is used in surgery, trauma care, and dehydration treatment. As a result, the affected containers are typically found in clinical settings rather than homes. That includes hospitals, surgical centers, clinics, and some infusion providers.
The FDA record lists the scope as 23,688 units. That is the quantity covered by this braun medical recall entry. The agency record does not list a full distribution map on the summary line. Typically, prescription IV fluids move through hospital distributors and group purchasing channels. However, readers should not assume distribution details that the agency did not publish.
The braun medical recall record does not include specific lot numbers in the summary text provided here. In most cases, the official notice carries the lot-level detail. Facilities should compare their inventory against the official listing rather than against any summary, including this one. The NDC and product code above are the starting points for that check.
The Hazard and Reported Injuries
The stated hazard in this braun medical recall is the presence of particulate matter. Particulate matter means unwanted solid particles inside the solution. In an IV bag, those particles can enter the bloodstream directly. There is no digestive tract or filter to stop them. That is why regulators treat injectable particulate seriously.
Potential clinical concerns with injected particulate are well documented in general medical literature. They can include local vein irritation and inflammatory reactions. In some scenarios, particles may lodge in small blood vessels. Risk typically depends on particle size, particle load, and the patient’s condition. Critically ill patients and those receiving large fluid volumes may face more exposure.
Whether injuries have been reported in connection with this recall is not stated in the agency record. As a result, this guide makes no claim either way. Do not read the Class I designation as proof that harm occurred. Class I reflects the agency’s assessment of potential consequences, not a count of victims.
| Recall Number | D-0832-2026 |
|---|---|
| Issuing Agency | U.S. Food and Drug Administration |
| Recall Date | September 2, 2026 |
| Company | B Braun Medical Inc |
| Product | Lactated Ringer’s Injection USP, 1000 mL EXCEL container, L7500, NDC 0264-7750-00 |
| Units Affected | 23,688 |
| Hazard | Presence of particulate matter |
| Severity Classification | Class I |
What To Do If You Own This Product
Stop using affected inventory first. That is the standard response to any Class I drug recall. Move suspect containers away from active clinical stock. Label them clearly so no one grabs them by mistake. Then verify what you actually have on hand.
To identify the product, check the NDC number 0264-7750-00 on the container label. Also check the product code L7500 and the 1000 mL EXCEL container format. Compare your lot numbers against the official notice. For example, a facility with multiple delivery dates may hold both affected and unaffected stock.
The remedy instructions for this braun medical recall are not restated here. The agency record contained remedy text that did not match the product, so it has been withheld from this guide. Follow the instructions in the official notice instead. You can review it here: FDA Enforcement Report — official recall notice
Facilities should also notify their pharmacy and risk management teams. In most cases, hospital pharmacies coordinate returns and documentation. Patients who received IV fluids and have concerns should speak with their treating clinician. Adverse events can also be reported to the FDA’s MedWatch program. Keep any packaging, labels, and records related to the braun medical recall.
📨 Get Free Mass Tort Guides Alerts
Free · No spam · Unsubscribe anytime
Does a Braun Medical Recall Mean You Can Sue?
No. A recall is not a lawsuit. A recall is a safety action taken by a company, sometimes with agency involvement. It removes or corrects a product in the marketplace. It does not decide fault, and it does not create a legal claim on its own.
A legal claim generally requires more than a defective product listing. Typically, it requires an actual injury. It also requires causation, meaning the product plausibly caused that specific harm. Documentation matters here. Medical records, treatment dates, and product identification all help establish the connection.
The existence of this braun medical recall does not confirm that anyone was hurt. It also does not confirm that any lawsuit has been filed over it. However, if you believe you were injured after receiving this product, you may be eligible to pursue a claim. That determination belongs to a licensed attorney reviewing your records.
No outcome is guaranteed. Deadlines called statutes of limitations also apply, and they vary by state. As a result, delay can eliminate options that were once available. A consultation with a qualified attorney is the appropriate next step for anyone weighing a claim tied to the braun medical recall.
How Recalls Connect to Mass Tort Cases
Recalls often become evidence in later litigation. They can show when a company learned of a problem. They can also show what the company told regulators and customers. For example, the Philips CPAP recall of 2021 involved sound-abatement foam degrading inside breathing devices. That recall and the related agency findings became central documents in the consolidated litigation that followed.
The Takata airbag recalls followed a similar pattern. Inflator failures triggered one of the largest automotive recalls in U.S. history. Recall records, testing data, and internal timelines were then examined in coordinated proceedings. However, neither example means every recall leads to litigation. Most recalls end quietly with corrected or returned product. A braun medical recall entry is a regulatory event first. Whether it ever becomes more than that depends on evidence that does not yet exist in the public agency record.
Frequently Asked Questions
What product is covered by this braun medical recall?
The FDA record lists Lactated Ringer’s Injection USP, 1000 mL EXCEL container, product code L7500, NDC 0264-7750-00. It is a prescription-only IV solution. The recall number is D-0832-2026.
What does Class I mean in this context?
Class I is the FDA’s most serious recall classification. It is used when the agency concludes that exposure could cause serious health consequences or death. It reflects potential risk, not a confirmed injury count.
How do I find out what to do with affected inventory?
Follow the instructions in the official FDA notice linked in this guide. The remedy details are not restated here because the summary record was inconsistent. Your pharmacy or supplier can also help confirm your next step for this braun medical recall.
Were You Injured by a Recalled Product?
A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.
Official Sources & Resources
Verify every recall against the issuing agency before acting:
- U.S. Food and Drug Administration: official recall database — the record of truth for this notice
- CPSC: cpsc.gov — household goods, toys, furniture, appliances
- FDA: fda.gov — food, drugs, and medical devices
- NHTSA: nhtsa.gov — vehicles, tires, and child car seats
- USDA FSIS: fsis.usda.gov — meat, poultry, and egg products
Content last reviewed September 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.
Related Guides
- All Product Recalls
- All Active MDL Cases
- Mass Tort Explainers
- Mass Tort Tips
- Tort Reform by State — 50-State Comparison
Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.