eSuction Small Cavity — Class II medical device recall Z-0270-2023
Terminated recall by Endo-Therapeutics, Inc., reported 2022-11-30, distributed in FL, PA. Improper device regulatory classification
| Recall number | Z-0270-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Endo-Therapeutics, Inc., Clearwater, FL, United States |
| Recall initiated | 2022-10-24 |
| Classified | 2022-11-18 |
| Reported by FDA | 2022-11-30 |
| Terminated | 2024-01-24 |
| Distributed | FL, PA |
| Quantity | 28 devices |
| UPC / GTIN / UDI-DI | 00816207021393 |
| Lot numbers | 447037, 447204 |
| Model numbers | ET2005 |
Product
eSuction Small Cavity, Model ET2005
Reason for recall
Improper device regulatory classification
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0270-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.