Class II — Endo-Therapeutics, Inc.
| Recalling firm | ENDO-THERAPEUTICS, INC. |
|---|---|
| Registered facility | ENDO-THERAPEUTICS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Improper device regulatory classification |
| Product | eSuction Small Cavity, Model ET2005 |
| Quantity | 28 devices |
| Distribution | US distribution to Florida and Pennsylvania |
| Initiated | 2022-10-24 |
| Classified | 2022-11-18 |
| Terminated | 2024-01-24 |
| Recall number | Z-0270-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Endo-Therapeutics, Inc. (Z-0270-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91074/
Alerts for ENDO-THERAPEUTICS, INC.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.