Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
eSuction Small Cavity Recalled by Endo-Therapeutics, Inc. Due to Improper device regulatory classification
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Endo-Therapeutics, Inc. directly.
Affected Products
eSuction Small Cavity, Model ET2005
Quantity: 28 devices
Why Was This Recalled?
Improper device regulatory classification
Where Was This Sold?
US distribution to Florida and Pennsylvania
About Endo-Therapeutics, Inc.
Endo-Therapeutics, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report