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Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
Recalled May 13, 2026 · FDA recall Z-2073-2026 · Katalyst Surgical
Hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors. · FDA Class II
Units
50 units
Sold at
Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Description
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Product
DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
Manufacturer(s)
Katalyst Surgical, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →