# FDA recall Z-0352-2023

> **ARROW INTERNATIONAL Inc.** · Class I · device recall initiated 2022-10-27.

## Product

Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-45703-PCAM1, g) ASK-45703-PCCH2, h) ASK-45703-PN; catheter introducer

## Reason for recall

There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.

## Distribution

US Distributor in states of: FL, GA, KY, OH, PA and WV.

## Key facts

- **Recall number:** Z-0352-2023
- **Recalling firm:** ARROW INTERNATIONAL Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-10-27
- **Report date:** 2022-12-21
- **Termination date:** 2024-10-07

- **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-0352-2023

## Citation

> AI Analytics. FDA recall Z-0352-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0352-2023. Source: US FDA. Licensed CC0.

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