Reported May 13, 2026 · Ongoing
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
Katalyst Surgical, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Katalyst Surgical, LLC · 722 Goddard Ave · Chesterfield, MO · 63005-1100
Is this the product you have?
- DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps
- Model/Catalog NumberDVF4016-25-S
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published DVF4016-25-S10840096205128Lot Code: UDI-DI: (01)10840096205128(11)250709(17)280709(10)M48801 DVF4016-25-S10840096205128Lot Number: M48801 Expiration Date: 07/09/2028 UDI-DI: (01)10840096205128(11)251010(17)281010(10)M49278 DVF4016-25-S10840096205128Lot Number: M49278 Expiration Date: 10/10/2028 UDI-DI: (01)10840096205128(11)250429(17)280429(10)M47582 DVF4016-25-S10840096205128Lot Number: M47582 Expiration Date: 04/29/2028 UDI-DI: (01)10840096205128(11)250527(17)280527(10)M48049 DVF4016-25-S10840096205128Lot Number: M48049 Expiration Date: 05/27/2028 UDI-DI: (01)10840096205128(11)251125(17)281125(10)M51038 — Lot Number: M451038 Expiration Date: 11/25/2028 - Amount recalled
- 90 units
This recall covers 12 products
The agency filed one notice per product. You are reading one of them; the other 11 are below.
Where it was sold
- Nationwide
Why it was recalled
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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