---
title: "eSuction Small Cavity, Model ET2005 — FDA record Z-0270-2023 | Is It on Recall"
description: "Improper device regulatory classification"
url: https://isitonrecall.com/recall/fda-device-z-0270-2023-esuction-small-cavity-model-et2005/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# eSuction Small Cavity, Model ET2005 — FDA record Z-0270-2023

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 24, 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**: eSuction Small Cavity, Model ET2005
- **Reason**: Improper device regulatory classification
- **Classification**: Class II
- **Recalling firm**: Endo-Therapeutics, Inc.
- **Quantity**: 28 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0270-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0270-2023%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 | Model Number: ET2005; UDI-DI: 00816207021393; Lot Numbers: 447037, 447204 |

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

## Distribution

US distribution to Florida and Pennsylvania

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)

## Dates in the source

- **Report date**: Nov 30, 2022
- **Recall initiation date**: Oct 24, 2022
- **Center classification date**: Nov 18, 2022
- **Termination date**: Jan 24, 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-0270-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Endo-Therapeutics, Inc. records](https://isitonrecall.com/brand/endo-therapeutics-inc/)