Arrow Percutaneous Sheath Introducer Recall: Incorrect Adhesive Manufacturing

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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 percutaneous sheath introducers with 7.5-8 Fr catheters (model ASK-09903-MGH3) because the liquid adhesive was incorrectly manufactured. This could potentially affect the device's safety and function.

Why it’s dangerous

The recall is due to a supplier notice about incorrect liquid adhesive manufacturing. This could lead to improper device function or safety issues during medical procedures.

Who’s affected

Healthcare professionals using the device for venous access and catheter introduction are most likely affected. Patients receiving these procedures may also be impacted.

How to tell if you have this one

Check for the product code ASK-09903-MGH3 and UDI code (01)10801902159127(17)270331(11)251203(10)33F25J0352. The batch number is 33F25K0130.

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 matches the recalled model.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The recall is due to a supplier notice that the liquid adhesive was incorrectly manufactured.

What should I do if I have this product?

The official recall notice does not specify a remedy or action steps for affected users.

Is there a risk of injury from this product?

The recall indicates a potential safety issue due to incorrect adhesive manufacturing, but specific injury risks are not described.

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-1912-2026 — Arrow Arrow

Hello,

I own a Arrow that is covered by recall Z-1912-2026 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-1912-2026 (March 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1912-2026 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 PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code:

Recall notice