FDA Device recall Z-0270-2023
eSuction Small Cavity, Model ET2005
- FDA Device
- Class II
- terminated
- Published 2022-11-30
On 2022-11-30 the FDA classified a Class II recall of eSuction Small Cavity, Model ET2005 by Endo Therapeutics, citing improper device regulatory classification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0270-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-10-24 |
| Published | 2022-11-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Endo Therapeutics |
| Distribution | FL, PA |
Product
eSuction Small Cavity, Model ET2005
Reason
Improper device regulatory classification
Identifiers
| code_info | Model Number: ET2005; UDI-DI: 00816207021393; Lot Numbers: 447037, 447204 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0270-2023%22
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