---
title: "Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheter... — FDA record Z-0351-2023 | Is It on Recall"
description: "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 Cen"
url: https://isitonrecall.com/recall/fda-device-z-0351-2023-arrow-mac-two-lumen-central-venous-access-kit-fr-use-with-7-7-5-fr-catheters-ref-ask-11242-upm1-cath/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer — FDA record Z-0351-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 27, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
- **Reason**: 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.
- **Classification**: Class I
- **Recalling firm**: ARROW INTERNATIONAL Inc.
- **Quantity**: 80 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0351-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0351-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 10801902159448, Lot Number 13F22C0349 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: Dec 21, 2022
- **Recall initiation date**: Oct 27, 2022
- **Center classification date**: Dec 9, 2022
- **Termination date**: Oct 7, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0351-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ARROW INTERNATIONAL Inc. records](https://isitonrecall.com/brand/arrow-international-inc/)