# FDA recall Z-2327-2017

> **Arrow International Inc** · Class II · device recall initiated 2017-05-09.

## Product

Arterial Catheterization Kit,   Arterial Line Kit with Sharps Safety Features  wire, guide, catheter  The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels

## Reason for recall

Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.

## Distribution

Worldwide Distribution - US (nationwide) and Canada

## Key facts

- **Recall number:** Z-2327-2017
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-09
- **Report date:** 2017-06-21
- **Termination date:** 2018-09-17

- **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-2327-2017

## Citation

> AI Analytics. FDA recall Z-2327-2017. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2327-2017. Source: US FDA. Licensed CC0.

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