Arrow MAC Two-Lumen Central Venous Access Kit Recall: Incorrect Adhesive Manufacturing

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Recalling firmARROW INTERNATIONAL, LLC3015 Carrington Mill Blvd, N/A · Morrisville, NC 27560-5437

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling MAC Two-Lumen Central Venous Access Kits for use with 7.5-8 Fr. catheters due to incorrect adhesive manufacturing. This could lead to improper device function or complications during medical procedures.

Why it’s dangerous

The liquid adhesive was incorrectly manufactured, which could cause improper sealing of the device. This might lead to leaks or infections during medical procedures, though the risk is not severe under normal use conditions.

Who’s affected

Healthcare professionals using the MAC Two-Lumen Central Venous Access Kit with specific UDI codes and batch numbers. Patients receiving procedures involving this kit may be at risk if the device malfunctions.

How to tell if you have this one

Check for the product code ASK-11142-LC2 and UDI code (01)10801902206807(17)270531(11)251211(10)33F25M0670. The batch number is 33F25M0670.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the product code and UDI code on the device to confirm if it is affected.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The liquid adhesive was incorrectly manufactured, which could cause improper sealing of the device.

What should I do if I have this product?

Contact Arrow directly for specific instructions on whether to stop using or return the product.

Is there a risk of serious injury?

The recall states the adhesive was incorrectly manufactured, but no specific injury risks are mentioned.

Take action

Contact Arrow

We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1916-2026 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1916-2026 from Arrow.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1916-2026 (March 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1916-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code:

Lower-risk recall