HIGH

Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen...

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

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

Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology permits short-term (<30 days) venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The Arrowg+ard technology is intended to help provide protection against catheterrelated infections. Clinical data have not been collected that demonstrate the use of the Arrowg+ard antimicrobial surface in decreasing catheter-related infections for this device. It is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use.. Reason: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured. Classification: Class II. Quantity: 95. Distribution: U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

Safety Guide

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Product Classification

Product Details

Model Numbers
Product Code: ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 Batch Number: 33F25M0671
Affected States
ALL
Report Date
April 29, 2026
Recall Status
ACTIVE

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