Recall Summary
| Recall number | Z-2370-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-06-24 |
| Company | ARROW INTERNATIONAL, LLC |
| Units affected | 37,738 |
| 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
arrow international recall notices reached hospitals and clinics in June 2026. The U.S. Food and Drug Administration classified this action as Class I. That is the agency’s most serious category. Arrow International, LLC recalled certain PICC kits and sets. These are catheter kits used for intravenous access. This guide explains the arrow international recall in plain language. It matters because these products are used in direct patient care.
What the Arrow International Recall Covers
The arrow international recall involves peripherally inserted central catheter kits. These are commonly called PICC kits. The recall also covers related PICC sets. Each kit is identified by a REF number. For example, one code is ASK-44063-NS. Another is ASK-45052-NS. The list also includes ASK-45541-MHBV and ASK-45552-RH. A NaviCurve variant carries the code DLX-45552-CURVB.
These kits come in different sizes. For example, some are 6 FR by 40 CM. Others are 5.5 FR by 55 CM. The sizes reflect the catheter gauge and length. Healthcare providers select a size based on the patient. The affected products were distributed for clinical use. In most cases, they reach hospitals, infusion centers, and similar facilities.
The FDA assigned this action recall number Z-2370-2026. The recall date is June 24, 2026. The scope covers 37,738 units. That is a large volume of medical devices. As a result, many care settings may hold affected stock. Providers should check their inventory against the REF codes above. The arrow international recall applies only to the listed kit and set numbers.
You will not find these kits on a store shelf. They are professional-use medical devices. Typically, a nurse or clinician handles them during a procedure. Patients rarely see the packaging directly. However, patients may still want to understand the arrow international recall. Knowing what was recalled helps you ask informed questions of your care team.
The Hazard and Reported Injuries
The hazard in the arrow international recall traces back to a supplier. The kits and sets included certain injectable drugs. These were lidocaine, bupivacaine, and 0.9% sodium chloride. All three came from a supplier that faced its own recall. The supplier was found to have quality issues. There were also limited reports of drug ineffectiveness.
The core safety concern involves sterility. These are water-based injectable products. If sterility is compromised, the risk rises sharply. Compromised sterility could lead to serious injury. In severe cases, it could become life-threatening. That risk is why the FDA used the Class I label. A Class I designation signals a reasonable probability of serious harm.
The agency record does not state whether injuries occurred. As a result, this guide makes no claim either way. We will not say injuries happened. We will also not say they did not. The arrow international recall record simply does not address that point. Readers should rely only on verified information. Do not assume harm that the record never confirms.
| Recall number | Z-2370-2026 |
| Issuing agency | U.S. Food and Drug Administration |
| Recall date | June 24, 2026 |
| Company | ARROW INTERNATIONAL, LLC |
| Units affected | 37,738 |
| Severity classification | Class I |
What To Do If You Own This Product
Start by checking your inventory. This step applies mainly to healthcare providers. Look for the REF codes tied to the arrow international recall. Match them against the kits on hand. For example, look for ASK-44063-NS or DLX-45552-CURVB. Set aside any product that matches. Do not use a recalled kit for patient care.
Next, follow the official notice. The remedy details belong to Arrow International and the FDA. This guide does not state the remedy steps. That is intentional and cautious. Instead, read the official instructions linked on this page. Follow those instructions exactly. They are the authoritative source for what to do next.
If you are a patient, talk to your care team. Ask whether your treatment used an affected kit. Your providers can check their records. Typically, facilities track device lot and REF information. However, do not panic based on the recall alone. The arrow international recall is a precautionary safety action.
Keep any paperwork you receive. Save discharge notes and device information. This record may matter later. For example, it could help a doctor answer questions. It could also help you understand your own care. In most cases, careful record-keeping is simply good practice. It costs nothing and can help you stay informed.
Does a Arrow International Recall Mean You Can Sue?
A recall is not a lawsuit. This is an important distinction. The arrow international recall is a safety action. It is a step to remove risky products from use. A recall alone does not create a legal claim. It is not the same as proof of harm. It is also not an admission of liability.
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To have a claim, more is usually needed. Typically, you must show an actual injury. You must also show that the product caused it. That link is called causation. Without injury and causation, a recall by itself is not a case. However, every situation is different. Only a professional can assess your specific facts.
If you believe you were harmed, seek advice. Speak with a licensed attorney in your state. A lawyer can review your medical records. They can explain your options honestly. You may be eligible to pursue a claim in some cases. However, no one can promise a result. Avoid anyone who guarantees money.
Be cautious with claims about compensation. No guide can tell you that you are owed anything. The arrow international recall does not entitle anyone to payment. Legal outcomes depend on facts and law. As a result, an individual review is essential. A qualified attorney is the right person to give it.
How Recalls Connect to Mass Tort Cases
A recall can become part of later litigation. It often serves as evidence. For example, a recall can show a company knew of a defect. It can also show when the problem was identified. However, a recall does not decide a case by itself. Courts still require proof of injury and causation.
History offers useful examples. The Philips CPAP recall led to extensive litigation over foam breakdown. The Takata airbag recall involved millions of vehicles and years of legal action. In both cases, the recall was a starting point, not a verdict. The arrow international recall may or may not follow a similar path. Only time and evidence will tell.
Frequently Asked Questions
Is the arrow international recall a Class I recall?
Yes. The FDA classified this action as Class I. That is the agency’s most serious category. It signals a reasonable probability of serious or life-threatening harm.
How many units are affected?
The recall covers 37,738 units. It carries recall number Z-2370-2026. The recall date is June 24, 2026.
Where can I find the official remedy instructions?
Read the official FDA notice linked on this page. This guide does not restate the remedy. Follow the instructions in that official notice exactly.
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.