# FDA recall Z-1152-2018

> **Arrow International Inc** · Class II · device recall initiated 2017-12-21.

## Product

ARROWg+ard Blue PLUS catheter, Catalog Number: ASK-45854-NG    Product Usage:  The ARROWg+ard Blue PLUS¿ catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins. 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

Certain lots may be missing information at the bottom of the lid including the lot number, expiration date, and Unique Device Identification (UDI) information.

## Distribution

United States in the state of  FL.

## Key facts

- **Recall number:** Z-1152-2018
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-21
- **Report date:** 2018-03-28
- **Termination date:** 2020-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reading, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1152-2018

## Citation

> AI Analytics. FDA recall Z-1152-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1152-2018. Source: US FDA. Licensed CC0.

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