Baxter Duo-Vent Solution Set and Male Luer Lock Adapter Recall: What To Do

A baxter healthcare recall issued in August 2026 involves IV solution administration sets used in hospitals and clinics. The U.S. Food and Drug Administration assigned it recall number Z-2766-2026 on August 19, 2026. Baxter Healthcare Corporation recalled its Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507. The FDA classified the action as Class I. That is the agency’s most serious category. It covers 24,528 units. If you or a family member received IV therapy recently, this guide explains what the recall means.

What the Baxter Healthcare Recall Covers

The baxter healthcare recall covers a specific IV delivery product. The recalled item is the Baxter Duo-Vent Solution Set and Male Luer Lock Adapter. The agency record lists Product Code 1C8507. The broader product category is solution administration sets.

Solution administration sets are the tubing systems that carry fluid from an IV bag to a patient. They typically include a drip chamber, tubing, a roller clamp, and a connector. The male luer lock adapter joins the set to a catheter or another line. In most cases, these sets are single-use and disposable.

The FDA record puts the scope of this baxter healthcare recall at 24,528 units. That is the number of affected products identified by the company and agency. The recall was dated August 19, 2026. Specific lot codes and distribution dates are listed in the official notice rather than summarized here.

These are professional-use medical devices. For example, they are typically used in hospitals, surgical centers, infusion clinics, and some home infusion settings. They are not sold in retail pharmacies to general consumers. As a result, most patients never handled the product directly. The facility providing care would have been the purchaser.

The Hazard and Reported Injuries

The hazard in this baxter healthcare recall involves air. Baxter received customer reports of air bubbles appearing in the drip chamber and in the tubing. According to the agency record, this happened when a pressure cuff was in use. It also happened when the tubing was flushed at the fully open position.

Air in an IV line is a known clinical concern. Clinicians are trained to prime lines and clear visible air before infusion. However, air that develops during pressurized infusion may be harder to catch in real time. Pressure cuffs are typically used when fluid must be delivered rapidly, such as during trauma care or surgery.

The FDA gave this recall a Class I classification. Class I is reserved for situations where the agency believes there is a reasonable probability that use of the product could cause serious adverse health consequences or death. That classification reflects the agency’s risk assessment of the defect. It is not, by itself, a finding that harm occurred.

Whether any injuries have been reported in connection with this baxter healthcare recall is not stated in the agency record reviewed for this guide. This guide does not claim that injuries occurred, and it does not claim that none did. Readers who want that detail should consult the official notice and their treating providers.

What To Do If You Own This Product

If your facility stocks this product, stop using the affected inventory. Quarantine it so it cannot be pulled during a busy shift. Then check your supply against Product Code 1C8507 and the identifiers listed in the official notice. Product codes and lot numbers are typically printed on the outer carton and the individual pouch.

The remedy instructions in the agency record for this recall did not match the recalled product, so they are not repeated here. Do not guess at the correction steps. Instead, follow the instructions in the official notice linked on this page. That notice is the controlling source for return, replacement, or correction procedures.

Official notice: FDA medical device recall database

Facility staff should also contact Baxter Healthcare Corporation directly through the contact information provided in the recall notice. Risk management and materials management should be looped in. In most cases, the manufacturer coordinates replacement stock so patient care is not interrupted. Document what you removed and when.

Patients are in a different position. You typically will not have this product at home. However, if you received IV therapy and experienced unexpected symptoms afterward, tell your doctor. Ask whether the device used in your care is covered by this baxter healthcare recall. You can also report a problem to the FDA through its MedWatch program.

Does a Baxter Healthcare Recall Mean You Can Sue?

No. A recall is not a lawsuit. A recall is a safety action taken by a company, sometimes at the FDA’s urging, to correct or remove a product from the market. It is a regulatory and corrective step. It is not a court finding that anyone was harmed or that anyone is legally liable.

The existence of this baxter healthcare recall does not, on its own, create a legal claim for any individual. This guide is not aware of any verified lawsuit filed over this specific recall, and it does not assert that one exists. A claim generally requires more than a defective product notice. It typically requires an actual injury.

In most cases, a product liability claim needs several elements. There must be a defect. There must be a real injury. And there must be causation, meaning the defect actually contributed to that injury. Proving causation in a medical device case usually requires medical records, device identification, and expert review. That is fact-specific work.

If you believe you were injured during an infusion, you may be eligible to pursue a claim. That depends entirely on your facts and on the law in your state. Talk to a licensed attorney who handles medical device cases. No one can promise you compensation, and no outcome is guaranteed. Deadlines called statutes of limitations can also apply.

How Recalls Connect to Mass Tort Cases

Recalls and lawsuits are separate, but they sometimes intersect. A recall notice creates a documented record. It shows what the defect was, when the company learned of it, and how many units were affected. In later litigation, plaintiffs’ attorneys often use that record as evidence of notice and of the defect’s nature.

History offers examples. Philips recalled millions of CPAP and ventilator devices starting in 2021 over degrading sound abatement foam. Thousands of individual claims were later consolidated into multidistrict litigation. Takata airbag inflators were recalled across many automakers, and that recall record featured heavily in the litigation and claims process that followed.

Those examples do not predict anything about this baxter healthcare recall. Many recalls never produce litigation at all. Most are handled quietly through replacement and correction. However, they show why a recall record matters. It preserves facts that might otherwise be difficult to establish years later.

Frequently Asked Questions

What product is covered by the baxter healthcare recall?

The recall covers the Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507, within the solution administration sets category. The FDA recall number is Z-2766-2026, dated August 19, 2026. It affects 24,528 units.

Why is this baxter healthcare recall classified as Class I?

Class I is the FDA’s most serious recall class. It applies when the agency finds a reasonable probability that using the product could cause serious health consequences or death. Here, the reported problem is air bubbles in the drip chamber and tubing under pressure cuff use or full-open flushing.

Have injuries been reported in this baxter healthcare recall?

The agency record reviewed for this guide does not state whether injuries were reported. We therefore make no claim in either direction. Check the official FDA notice for the most current information, and speak with your healthcare provider about your own care.

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 August 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.

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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.