---
title: "Atrium Firm PVC Thoracic Catheter 36FR Straight, part number 15036. — FDA record Z-0484-2024 | Is It on Recall"
description: "A sterilization nonconformance prematurely aged the product, resulting in an inaccurate labeled expiration date."
url: https://isitonrecall.com/recall/fda-device-z-0484-2024-atrium-firm-pvc-thoracic-catheter-36fr-straight-part-number-15036/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Atrium Firm PVC Thoracic Catheter 36FR Straight, part number 15036. — FDA record Z-0484-2024

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 Sep 29, 2023. 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**: Atrium Firm PVC Thoracic Catheter 36FR Straight, part number 15036.
- **Reason**: A sterilization nonconformance prematurely aged the product, resulting in an inaccurate labeled expiration date.
- **Classification**: Class II
- **Recalling firm**: Atrium Medical Corporation
- **Quantity**: 2460 units (246 cases, 10 units/case)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0484-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0484-2024%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: 00650862150360, lot ME234686, expiration date 2023-02-24. |

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

## Distribution

US: AL, AZ, CA, FL, IA, IL, IN, MD, MI, MN, NJ, PA, TN & TX

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

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Dec 13, 2023
- **Recall initiation date**: Sep 29, 2023
- **Center classification date**: Dec 1, 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-0484-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Atrium Medical Corporation records](https://isitonrecall.com/brand/atrium-medical-corporation/)