Recall Summary
| Recall number | Z-2379-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-06-24 |
| Company | ARROW INTERNATIONAL, LLC |
| Units affected | 1,516 |
| 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
The arrow international recall is a Class I safety action issued in June 2026. The U.S. Food and Drug Administration flagged the event under recall number Z-2379-2026. It affects certain Arrow International, LLC procedure kits used in clinical settings. These kits contained recalled anesthetic and saline components from a supplier. This matters because a Class I designation is the most serious category. It signals a reasonable chance of serious or life-threatening harm. If you or a loved one received care involving these kits, this guide explains what happened.
What the Arrow International Recall Covers
The arrow international recall covers a group of “PI JACC” and “AGBA PI JACC” procedure kits. These are pain-management and catheter kits used by medical providers. The affected reference numbers include ASK-41552-LTAC and ASK-42063-LTAC. They also include CDC-41541-JX1A, CDC-41552-JX1A, and CDC-41563-JX1A. The kits came in several sizes and French-gauge configurations. In most cases, hospitals and clinics ordered these directly from the manufacturer.
Arrow International, LLC issued the recall through the FDA on June 24, 2026. The scope covers 1,516 units in total. That is a relatively small number of kits. However, a small unit count does not lower the severity. The FDA still classified this as Class I. As a result, providers were expected to act quickly to identify affected stock.
These products are not sold to consumers on store shelves. Instead, they are professional medical devices. For example, a hospital pharmacy or procedure suite would stock them. If you were treated with one, the kit would have been used by clinical staff. Typically, patients would not handle the packaging or reference numbers themselves. That is why checking with your provider is the practical first step.
The Hazard and Reported Injuries
The core problem in the arrow international recall involves included drug components. The kits contained Lidocaine, Bupivacaine, and 0.9% sodium chloride. Those items were themselves the subject of a separate supplier recall. The supplier was found to have quality issues. There were also limited reports of drug ineffectiveness tied to that supplier.
The deeper concern is sterility. These are water-based injectable products. If the sterility of such a product is compromised, the risk rises sharply. In most cases, contamination of an injectable can lead to serious infection. As a result, the FDA warned this could cause serious or life-threatening injuries. That risk is what drove the Class I classification.
Importantly, the agency record does not state whether any injuries were actually reported. So this guide will not claim that people were harmed. It also will not claim that no one was harmed. The FDA record simply does not say. Typically, a Class I label reflects potential risk, not a confirmed injury count. The table below summarizes the verified agency facts for quick reference.
| Detail | Information |
|---|---|
| Recall Number | Z-2379-2026 |
| Issuing Agency | U.S. Food and Drug Administration |
| Recall Date | June 24, 2026 |
| Company | Arrow International, LLC |
| Units Affected | 1,516 |
| Severity | Class I |
What To Do If You Own This Product
If you are a provider, stop using any affected inventory now. First, check your stock against the reference numbers listed above. For example, look for ASK-41552-LTAC or the CDC-JX1A series codes. Then quarantine any matching kits so they are not used on patients. Typically, facilities log recalled lots and remove them from active supply.
The specific corrective steps for the arrow international recall must come from the official notice. The remedy details in the agency file did not match the product cleanly. As a result, we are not stating the remedy here. Instead, follow the exact instructions in the FDA notice linked on this page. That notice is the authoritative source for returns, replacement, or disposal.
Patients cannot easily identify these kits on their own. However, you can still take action. Ask your hospital or clinic whether your care involved a recalled Arrow International kit. Keep any paperwork, discharge notes, or billing records you have. In most cases, your medical team can confirm which products were used. Review the official notice below for the current provider instructions.
Here is the official FDA recall notice for reference.
View the official FDA recall notice
Does a Arrow International Recall Mean You Can Sue?
A recall is a safety action. It is not a lawsuit. This point matters, so we will say it plainly. The arrow international recall does not, by itself, create a legal claim. It is the manufacturer and FDA working to remove a risk. In most cases, a recall is about prevention, not blame.
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A legal claim usually needs more than a recall. Typically, it requires an actual injury. It also requires a link between that injury and the product. Lawyers call that link “causation.” Without documented harm and causation, a recall alone is not a case. As a result, the recall number is only one piece of any potential claim.
If you believe you were harmed, speak with a licensed attorney. An attorney can review your medical records and the timeline. They can tell you whether you may be eligible to pursue a claim. However, no one can promise an outcome. You are not automatically owed anything because a recall exists. Every situation depends on its own facts.
How Recalls Connect to Mass Tort Cases
Recalls and mass torts are separate, but they can overlap over time. A recall documents that a product had a defect or risk. Later, if many people report similar injuries, lawyers may investigate. For example, the Philips CPAP recall in 2021 preceded large-scale litigation. The recall records became useful background evidence in those cases.
The Takata airbag recall followed a similar path. It was one of the largest recalls in history. Over time, injury reports and recall data helped support mass tort claims. However, this does not mean the arrow international recall will lead to litigation. As of now, we have not verified any lawsuit over this specific recall. Typically, a recall is just the starting point for further review, nothing more.
Frequently Asked Questions
Is the arrow international recall a Class I recall?
Yes. The FDA classified it as Class I under recall number Z-2379-2026. That is the most serious recall category. It reflects a chance of serious or life-threatening harm.
How many units are affected by the arrow international recall?
The recall covers 1,516 units. These are professional medical procedure kits. They were distributed to clinical settings, not sold directly to consumers.
Does the arrow international recall mean someone was injured?
The FDA record does not state whether injuries were reported. So we cannot say either way. The Class I label reflects potential risk, not a confirmed injury count.
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.