Z-2072-2026Class II

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

Name: Z-2072-2026 DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
Creator: Katalyst Surgical, LLC
Published: 2026-03-25
License: https://open.fda.gov/license/

Katalyst Surgical, LLC / initiated 2026-03-25 / Open, Classified / root cause: labeling and UDI

FDA source

Katalyst Surgical, LLC began a recall of DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S on 2026-03-25. FDA classified it as Class II and gives the reason as "Field Safety Corrective Action for IFU in DEX Forceps and Scissors". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-2072-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-03-25
Posted: 2026-05-06
Recalling firm: Katalyst Surgical, LLC
Product: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
Product code: HNR Forceps, Ophthalmic
Reason for recall: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Root cause tag: labeling and UDI
FDA root cause: Under Investigation by firm
Action: A Field Safety Notification: Field Safety Corrective Action for IFU in DEX Forceps and Scissors dated 3/19/26 was sent to customers. FIELD SAFETY ACTIONS REQUIRED As a customer identified in the receipt of one or more of the affected lots, you are requested/required to take the following steps: 1. Please confirm receipt of this Field Safety Notification by email, either by replying to the sender or using the email addresses listed in the signature at the bottom of this notice. 2. Review the Individualized List of Affected Lot Numbers by Customer provided in the email for lots that were distributed to your facility. Identify all of these lots that currently remain in your stock and place them on hold. 3. Provide information to Katalyst Surgical team identifying which lots are currently in stock and on hold at your facility. Katalyst Surgical will send a replacement correct IFU for each affected box. 4. Upon receipt of the correct IFU, remove the incorrect IFU, replace the correct IFU in the box, and destroy the incorrect IFU. Approval for Modification including instructions will accompany the replacement IFUs. 5. We recommend you reach out to your customers/users of these DEX products with this information. Katalyst Surgical will gladly provide correct replacement IFU documents to you for further distribution. Katalyst Surgical deeply regrets the inconvenience this causes. We assure you of our continuous support and commitment to safety and quality. Please do not hesitate to contact our team if you have any further questions.
Quantity in commerce: 90 units
Distribution: Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Product codes and lots: 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

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2072-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2069-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2070-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2071-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2072-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2073-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2074-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2075-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2076-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2077-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2078-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2079-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06
Z-2080-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-13	2026-05-06

Product code HNR

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)