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FDA (Device enforcement)Recalled 2026-03-25class ii

Katalyst Surgical, LLC: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S

Hazard

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

Details from the source

Reason for recall: Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. Quantity: 90 units Lot/code info: Lot Code: Model No:DVF4016-25-S UDI-DI: (01)10840096205128(11)250709(17)280709(10)M48801 Lot Number: M48801 Expiration Date: 07/09/2028 Model No: DVF4016-25-S UDI-DI: (01)10840096205128(11)251010(17)281010(10)M49278 Lot Number: M49278 Expiration Date: 10/10/2028 Model No: DVF4016-25-S UDI-DI: (01)10840096205128(11)250429(17)280429(10)M47582 Lot Number: M47582 Expiration Date: 04/29/2028 Model No: DVF4016-25-S UDI-DI: (01)10840096205128(11)250527(17)280527(10)M48049 Lot Number: M48049 Expiration Date: 05/27/2028 Model No: DVF4016-25-S UDI-DI: (01)10840096205128(11)251125(17)281125(10)M51038 Lot Number: M451038 Expiration Date: 11/25/2028

UPC codes

10840096205128

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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