# FDA recall Z-2556-2019

> **Arrow International Inc** · Class II · device recall initiated 2019-08-06.

## Product

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit  Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.

## Reason for recall

Products may contain the incorrect banner card within the kit

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2556-2019
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-06
- **Report date:** 2019-10-02
- **Termination date:** 2020-09-29

- **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-2556-2019

## Citation

> AI Analytics. FDA recall Z-2556-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2556-2019. Source: US FDA. Licensed CC0.

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