Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27

Recall date

March 25, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2080-2026

FDA classification

Class II

Brand / firm

Katalyst Surgical, LLC

Sold / distributed

Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.

Why it was recalled

Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding tissues during surgical procedures. These devices fall under the GMDN code 62478 entitled Ophthalmic soft-tissue surgical forceps, probe-like, single use . Double pouched in tyvek pouches, sold in boxes of 5 with an inner and outer box.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27