# FDA recall Z-1914-2026

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

## Product

ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL  VENOUS CATHETER     REF ASK-42802-PLH  UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140    REF ASK-45703-MGH  UDI code: (01)10801902223675(17)261231(11)251209(10)33F25L0143    REF ASK-42854-MGH  UDI code: (01)10801902223668(17)261231(11)251210(10)33F25L0144    REF ASK-45854-MGH  UDI code: (01)10801902223699(17)261231(11)251209(10)33F25L0145    The Arrowg+ard technology is intended to provide protection against catheter-related  bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing  infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness  of the Arrowg+ard Blue Plus catheter in preventing CRBSIs compared to the original  Arrowg+ard Blue¿ catheter has not been studied.

## 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-1914-2026
- **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-1914-2026

## Citation

> AI Analytics. FDA recall Z-1914-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1914-2026. Source: US FDA. Licensed CC0.

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