{"url_path":"/fda/device/recalls/Z-2069-2026","section_key":"summary","section_title":"DEVICE Recall: Katalyst Surgical, LLC — DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-25","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2069-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Katalyst Surgical, LLC"},"word_count":84,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2069-2026\n\n**Recalling firm:** Katalyst Surgical, LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-25\n**Report date:** 2026-05-13\n\n## Product\nDEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23\n\n## Reason\nField Safety Corrective Action for IFU in DEX Forceps and Scissors.\n\n## Affected lots\nLot Code: Model No: DVF4005-23 UDI-DI: (01)10817489021658(11)250924(17)280924(10)M50529 Lot Number: M50529 Expiration Date: 09/04/2028\n\n## Distribution\nWorldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France."}