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 / numberBarcodesProduct 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.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Katalyst Surgical, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.