---
title: "EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012 — FDA record Z-1832-2024 | Is It on Recall"
description: "Devices may contain elevated levels of bacterial endotoxin."
url: https://isitonrecall.com/recall/fda-device-z-1832-2024-echotip-ultra-hd-endoscopic-ultrasound-access-needle-echo-hd-19-a-g52012/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012 — FDA record Z-1832-2024

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 Apr 1, 2024. 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**: EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012
- **Reason**: Devices may contain elevated levels of bacterial endotoxin.
- **Classification**: Class II
- **Recalling firm**: Cook Medical Incorporated
- **Quantity**: 1 Unit OUS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1832-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1832-2024%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 | Catalogue Number: ECHO-HD-19-A; GPN: G52012; UDI/DI: 00827002520127; Lot Numbers: C2145003 and C2144407. |

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

## Distribution

International distribution in the countries of Germany, Netherlands, Switzerland, United Kingdom.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: May 22, 2024
- **Recall initiation date**: Apr 1, 2024
- **Center classification date**: May 16, 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-1832-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cook Medical Incorporated records](https://isitonrecall.com/brand/cook-medical-incorporated/)