# FDA recall Z-0270-2023

> **Endo-Therapeutics, Inc.** · Class II · device recall initiated 2022-10-24.

## Product

eSuction Small Cavity, Model ET2005

## Reason for recall

Improper device regulatory classification

## Distribution

US distribution to Florida and Pennsylvania

## Key facts

- **Recall number:** Z-0270-2023
- **Recalling firm:** Endo-Therapeutics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-10-24
- **Report date:** 2022-11-30
- **Termination date:** 2024-01-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Clearwater, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0270-2023

## Citation

> AI Analytics. FDA recall Z-0270-2023. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0270-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*