---
title: "Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Num... — FDA record Z-3111-2026 | Is It on Recall"
description: "An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters."
url: https://isitonrecall.com/recall/fda-device-z-3111-2026-getinge-pvc-thoracic-catheter-soft-pvc-straight-10-per-case-size-model-number-1-16fr-8016-2-24fr-802/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 2... — FDA record Z-3111-2026

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 Aug 7, 2026. 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**: Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);
- **Reason**: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.
- **Classification**: Class II
- **Recalling firm**: Atrium Medical Corporation
- **Quantity**: 3618
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3111-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%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 | 1. Model Number(Size): 8016(16FR); UDI-DI: 00650862130164; Lot Number: ME244878; 2. Model Number(Size): 8024(24FR); UDI-DI: 00650862130249; Lot Number: ME244835; 3. Model Number(Size): 8028(28FR); UDI-DI: 00650862130287; Lot Numbers: ME244682, ME244836, ME244837, ME244681; 4. Model Number(Size): 8032(32FR); UDI-DI: 00650862130324; Lot Number: ME244840; 5. Model Number(Size): 8036(36FR); UDI-DI: 00650862130362; Lot Number: ME244686; |

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

## Distribution

US Nationwide distribution.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Sep 16, 2026
- **Recall initiation date**: Aug 7, 2026
- **Center classification date**: Sep 4, 2026

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-3111-2026%22)

## Related records

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