---
title: "Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), ... — FDA record Z-0464-2023 | Is It on Recall"
description: "The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits."
url: https://isitonrecall.com/recall/fda-device-z-0464-2023-medical-action-industries-inc-port-access-kit-ref-76511b-on-case-label-sterile-and-medical-action-in/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries I... — FDA record Z-0464-2023

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 12, 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**: Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit components are the Port Access Kit.
- **Reason**: The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
- **Classification**: Class II
- **Recalling firm**: Medical Action Industries, Inc. 306
- **Quantity**: 24 cases (480 kits)
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0464-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0464-2023%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 | Port Access Kit case label - Lot 294281, exp. 9/28/2023, UDI #1080916018095. IV Start Kit label - Lot 294589, exp. 12/20/2024, UDI #20809160195991. |

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

## Distribution

Distribution was made to MN. There was no foreign/government/military distribution.

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

- [Minnesota](https://isitonrecall.com/state/minnesota/)

## Dates in the source

- **Report date**: Dec 14, 2022
- **Recall initiation date**: Oct 12, 2022
- **Center classification date**: Dec 8, 2022
- **Termination date**: Mar 25, 2025

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-0464-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Action Industries, Inc. 306 records](https://isitonrecall.com/brand/medical-action-industries-inc-306/)