Arrowg+ard Blue MAC Two-Lumen Catheter Kit Recall: Incorrect Adhesive Manufacturing

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Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Arrow is recalling two-lumen central venous access kits that were manufactured with incorrect adhesive. This could affect the kit's ability to function properly during medical procedures.

Why it’s dangerous

The recall is due to a supplier error where the liquid adhesive was incorrectly manufactured. This could potentially affect the kit's performance during medical procedures, but there is no indication of immediate harm or injury.

Who’s affected

Healthcare professionals using the Arrowg+ard Blue MAC Two-Lumen Central Venous Access Kit for short-term catheter procedures are likely affected. Patients receiving these kits are at minimal risk due to the nature of the issue.

How to tell if you have this one

Check for the product code ASK-21142-DMC and UDI code (01)10801902218930(17)270630(11)251211(10)33F25M0671. The kit is sold for short-term use with 7.5-8 Fr. catheters.

Brand
Arrow
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the product code ASK-21142-DMC and UDI code (01)10801902218930(17)270630(11)251211(10)33F25M0671 to confirm if the kit is recalled.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to a supplier error with the adhesive, but there is no indication of immediate harm or injury. The product may not function properly.

What should I do if I have this product?

The official recall does not specify a remedy, so check the product details to confirm if it is recalled.

How can I tell if I have the recalled product?

Look for the product code ASK-21142-DMC and UDI code (01)10801902218930(17)270630(11)251211(10)33F25M0671 on the kit.

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-1917-2026 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1917-2026 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-1917-2026 (March 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1917-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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 Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI

Lower-risk recall