--- title: "Katalyst Surgical, LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Katalyst Surgical, LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/katalyst-surgical-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Katalyst Surgical, LLC recall records **12** reported ongoing 12 records in this archive. Latest source date Mar 25, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23](https://isitonrecall.com/recall/fda-device-z-2069-2026-dex-ophthalmic-tissue-forceps-23ga-dex-nanotapered-awh-forceps-model-catalog-number-dvf4005-23/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2069-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25](https://isitonrecall.com/recall/fda-device-z-2070-2026-dex-ophthalmic-tissue-forceps-25ga-dex-nano-tapered-awh-forceps-model-catalog-number-dvf4005-25/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2070-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S](https://isitonrecall.com/recall/fda-device-z-2071-2026-dex-ophthalmic-tissue-forceps-25ga-dex-stiff-asymmetrical-tano-forceps-model-catalog-number-dvf4014/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DV...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2071-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S](https://isitonrecall.com/recall/fda-device-z-2072-2026-dex-ophthalmic-tissue-forceps-25ga-dex-stiff-serrated-forceps-model-catalog-number-dvf4016-25-s/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2072-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23](https://isitonrecall.com/recall/fda-device-z-2073-2026-dex-ophthalmic-tissue-forceps-23ga-dex-maculorhexis-forceps-model-catalog-number-dvf4019-23/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2073-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25](https://isitonrecall.com/recall/fda-device-z-2074-2026-dex-ophthalmic-tissue-forceps-25ga-dex-maculorhexis-forceps-model-catalog-number-dvf4019-25/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2074-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S](https://isitonrecall.com/recall/fda-device-z-2075-2026-dex-ophthalmic-tissue-forceps-25ga-dex-stiff-maculorhexis-forceps-model-catalog-number-dvf4019-25-s/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2075-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27](https://isitonrecall.com/recall/fda-device-z-2076-2026-dex-ophthalmic-tissue-forceps-27ga-dex-stiff-maculorhexis-forceps-model-catalog-number-dvf4019-27/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2076-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S](https://isitonrecall.com/recall/fda-device-z-2077-2026-dex-ophthalmic-tissue-forceps-25ga-dex-stiff-end-grasping-forceps-model-catalog-number-dvf4022-25-s/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2077-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25](https://isitonrecall.com/recall/fda-device-z-2078-2026-dex-ophthalmic-tissue-forceps-25ga-dex-super-grip-forceps-model-catalog-number-dvf4034-25/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2078-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S](https://isitonrecall.com/recall/fda-device-z-2079-2026-dex-ophthalmic-tissue-forceps-25ga-dex-stiff-super-grip-forceps-model-catalog-number-dvf4034-25-s/) Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2079-2026%22) Mar 25, 2026 FDA device enforcement ### [DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27](https://isitonrecall.com/recall/fda-device-z-2080-2026-dex-ophthalmic-tissue-forceps-27ga-dex-stiff-super-grip-forceps-model-catalog-number-dvf4034-27/) 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 6... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. [Official source for DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2080-2026%22) ## Reasons in these listed records - Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - 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 Ophtha... These examples come from this result page and are not a ranking of every recall reason. ## Checking Katalyst Surgical, LLC ### Is there a recall on katalyst surgical, llc right now? This archive contains 12 records, including 12 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Katalyst Surgical, LLC](https://isitonrecall.com/check/?q=Katalyst%20Surgical%2C%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)