---
title: "HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access ( — FDA record Z-1156-2023 | Is It on Recall"
description: "Label with the incorrect component listed on the inner kit Tyvek header bag"
url: https://isitonrecall.com/recall/fda-device-z-1156-2023-hydromid-4fr-single-lumen-maximal-barrier-kit-indicated-for-short-term-access/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access ( — FDA record Z-1156-2023

Reported ongoing

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 Dec 22, 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**: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (
- **Reason**: Label with the incorrect component listed on the inner kit Tyvek header bag
- **Classification**: Class II
- **Recalling firm**: Access Vascular, Inc
- **Quantity**: 445 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1156-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1156-2023%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: (01)00850030354020 Lot Numbers: 11424032, 11432076 |

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

## Distribution

US Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Nebraska](https://isitonrecall.com/state/nebraska/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Mar 1, 2023
- **Recall initiation date**: Dec 22, 2022
- **Center classification date**: Feb 22, 2023

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-1156-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Access Vascular, Inc records](https://isitonrecall.com/brand/access-vascular-inc/)