Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC Recall: What To Do

arrow international recall information now applies to a medical device kit used in hospitals and clinics. The U.S. Food and Drug Administration lists this action under recall number Z-2387-2026. The recalling company is ARROW INTERNATIONAL, LLC. The agency dated the record June 24, 2026. Regulators classified it as Class I. That is the most serious category the FDA uses. Most patients never handle these kits themselves. However, clinicians, purchasing staff, and families still deserve a clear explanation.

What the Arrow International Recall Covers

The arrow international recall covers one specific product configuration. The agency record lists the description and reference exactly as follows: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC. That describes a midline catheter kit. The catheter measures 5 French in diameter and 20 centimeters in length. The “2L” indicates a two-lumen design. The code CDC-32052-MPKC identifies the packaged configuration. Nothing outside that description is part of this particular record.

Midline catheters sit between a standard IV and a central line. Clinicians place them in an arm vein for medium-term access. Typically, they support therapy lasting several days to a few weeks. Kits like this one bundle the catheter with the supplies needed for placement. For example, a kit may include local anesthetic and flush solution. That bundling detail matters here. It is the reason this arrow international recall was issued at all.

The scope listed by the agency is 90 units. That is a small distribution footprint. However, a small unit count does not reduce the severity rating. Class I reflects the potential consequence, not the quantity. As a result, facilities holding even one affected kit should treat the notice seriously. In most cases, hospital materials management teams receive these notices directly from the manufacturer or distributor.

The public agency summary for this arrow international recall does not publish lot numbers or sale dates. It also does not list individual distribution sites. Therefore, this guide will not guess at them. Facilities should confirm affected inventory using the reference code and the official notice. Products of this type are generally supplied to hospitals, surgical centers, and clinics. They are not sold to consumers at retail.

The Hazard and Reported Injuries

The hazard described by the FDA does not concern the catheter itself. It concerns drug components placed inside the kits. According to the agency, lidocaine, bupivacaine, and 0.9% sodium chloride were included into kits and sets. Those items were the subject of a separate supplier recall. The supplier was found to have quality issues. The agency also cites limited reports of drug ineffectiveness tied to that supplier.

Sterility is the central concern. The agency states that these are water-based injectable products. If sterility of such a product is compromised, contamination becomes possible. That contamination can enter the bloodstream during a procedure. As a result, the FDA warns this could lead to serious or life-threatening injuries. For example, bloodstream infections in hospitalized patients can escalate quickly. Ineffective local anesthetic raises a second, separate concern about pain control during placement.

The agency record does not state whether any injuries occurred from these specific units. This guide will not claim that injuries happened. It also will not claim that none happened. Readers should rely on the official notice and their own medical providers. Typically, adverse events tied to a device are reported through the FDA MedWatch system. Below is a summary of the verified record for this arrow international recall.

What To Do If You Own This Product

Start by stopping use. Any kit matching the recalled description should be pulled from active stock. Move it to a clearly labeled quarantine area. That prevents accidental use during a busy shift. In most cases, hospitals already have a documented recall quarantine process. Follow it exactly. Do not return the item to general inventory until the manufacturer confirms the correct disposition.

Next, identify the product carefully. Match the reference code CDC-32052-MPKC against your shelf labels and purchase records. Check both central supply and satellite storage areas. For example, procedure carts and clinic cabinets are easy to overlook. Compare your findings against any notice received from the distributor. If the code does not match, the item is likely outside this arrow international recall. When unsure, contact the manufacturer before use.

This guide does not state the remedy for this action. The agency record contains remedy text that does not match the product, so it has been withheld here. Follow the instructions in the official notice linked on this page instead. That notice is the authoritative source for next steps. Do not improvise a return, replacement, or disposal process. Your distributor representative can confirm the correct procedure for your facility.

View the official FDA recall notice

Patients have a simpler path. You will rarely know which kit was used during your procedure. However, you can ask. Request your procedure records from the facility. Ask whether a recalled midline kit was involved. If you developed an infection or unusual symptoms afterward, speak with a physician promptly. Keep copies of every record. Documentation matters far more than memory if questions arise later about this arrow international recall.

Does a Arrow International Recall Mean You Can Sue?

A recall is not a lawsuit. That distinction is important and often misunderstood. A recall is a safety action. It removes or corrects a product that may present a risk. Regulators and manufacturers use recalls to prevent harm before it happens. As a result, the existence of this arrow international recall does not by itself create a legal claim for anyone.

A personal injury claim generally requires more than a defect notice. Typically, it requires an actual injury. It also requires a link between the product and that injury. Lawyers call that causation. Medical records, procedure notes, and product identification all help establish it. Without those pieces, a recall notice is simply a safety bulletin. In most cases, that is exactly what it remains.

If you were treated with an affected kit and later suffered harm, you may be eligible to pursue a claim. That is a possibility, not a promise. No one can tell you what your case is worth from a web page. A licensed attorney in your state can review the facts. Deadlines called statutes of limitation also apply and vary widely. However, nothing here guarantees compensation or predicts any outcome.

How Recalls Connect to Mass Tort Cases

Recalls sometimes become evidence in later litigation. They can show what a company knew and when it acted. For example, the 2021 Philips CPAP and ventilator recall involved sound abatement foam that could degrade. Thousands of users later filed claims, and courts consolidated them into multidistrict litigation. The recall documents became part of the factual record. However, the recall itself was not the claim.

The Takata airbag inflator recalls followed a similar pattern. Those recalls became among the largest automotive safety actions in United States history. Litigation followed separately, driven by reported injuries and alleged defect knowledge. In both examples, the recall was a starting point for investigation. As a result, plaintiffs still had to prove injury and causation individually. The same principle applies to any arrow international recall discussion today.

Frequently Asked Questions

What does a Class I classification mean in this arrow international recall?

Class I is the FDA’s most serious recall category. It means there is a reasonable probability that use could cause serious health consequences or death. The classification reflects potential risk, not confirmed harm in any specific patient.

Were any injuries reported from these 90 units?

The agency record does not state whether injuries were reported. This guide will not claim that injuries occurred or that none occurred. Patients with concerns should speak with their treating physician and review their procedure records.

How do I know if my facility has affected inventory?

Check your stock and purchase records against the reference code CDC-32052-MPKC. Search central supply, clinic storage, and procedure carts. Then follow the instructions in the official FDA notice linked above, and confirm with your distributor if anything is unclear.

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 July 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.