Which brands are affected?

The following brands are affected: ARROW INTERNATIONAL.

HIGHMarch 11, 2026

PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous...

Q: Which model numbers are affected?

Affected models: Product code:ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130.

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Quick Facts at a Glance

Recall Date: March 11, 2026
Hazard Level: HIGH
Brand: ARROW INTERNATIONAL
Geographic Scope: 1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

1Stop using the product until you confirm whether it is included in the recall.
2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand: ARROW INTERNATIONAL
Model numbers: Product code:ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130
Where affected: ALL

Hazard Information

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact ARROW INTERNATIONAL, LLC or your healthcare provider for instructions. Notification method: Letter

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Full Description

PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.. Reason: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured. Classification: Class II. Quantity: 115. Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

View Original Recall on FDA - Medical Devices