# FDA recall Z-1915-2026

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

## Product

Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1  UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011    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-1915-2026
- **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-1915-2026

## Citation

> AI Analytics. FDA recall Z-1915-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1915-2026. Source: US FDA. Licensed CC0.

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