FDAOctober 24, 2022device

eSuction Small Cavity, Model ET2005

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Improper device regulatory classification

What to do

FDA enforcement status: Terminated

Brands named

endo therapeuticsendoendo therapeutics

UPCs

00816207021393

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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