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Endo-Therapeutics, Inc. recalls eSuction Small Cavity, Model ET2005
Recalled November 30, 2022 · FDA recall Z-0270-2023 · Endo-Therapeutics
Hazard
Improper device regulatory classification · FDA Class II
Units
28 devices
Sold at
US distribution to Florida and Pennsylvania
Description
Improper device regulatory classification
Product
eSuction Small Cavity, Model ET2005
Manufacturer(s)
Endo-Therapeutics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →