FDA DeviceClass IINotable

FDA Recall: DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23

Date: 2026-05-13
Brand: Katalyst Surgical, LLC
Category: Medical Device
FDA Class: Class II

Description

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Hazard

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Remedy

5 units

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