Recall Z-0270-2023— Endo-Therapeutics, Inc.

Name: FDA recall Z-0270-2023
Creator: U.S. Food and Drug Administration
Published: 2022-10-24

Class II · Terminated

Class II FDA medical device recall by Endo-Therapeutics, Inc., initiated 2022-10-24, terminated 2024-01-24. FDA's recall record names no specific 510(k) clearance for this event. Product: eSuction Small Cavity, Model ET2005. Reason: Improper device regulatory classification.

Recalling firm: Endo-Therapeutics, Inc.
Classification: Class II
Status: Terminated
Initiated: 2022-10-24
Terminated: 2024-01-24
Firm location: Clearwater, FL, United States

Product description

eSuction Small Cavity, Model ET2005

Reason for recall

Improper device regulatory classification

Data sourced from openFDA. This site is unofficial and independent of the FDA.