# FDA recall Z-1917-2026

> **ARROW INTERNATIONAL, LLC** · Class II · device recall initiated 2026-03-11.

## Product

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 for recall

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

## Distribution

U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

## Key facts

- **Recall number:** Z-1917-2026
- **Recalling firm:** ARROW INTERNATIONAL, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-11
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1917-2026

## Citation

> AI Analytics. FDA recall Z-1917-2026. Retrieved 2026-08-02 from https://api.ai-analytics.org/recall/Z-1917-2026. Source: US FDA. Licensed CC0.

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