FDA DevicesClass II
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Nu...
Published: May 13, 2026Recall ID: Z-2072-2026Category: devicesCountry: US
Reason for Recall / Hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Product Description & Identification
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
Additional Source Details
| Field | Value |
|---|---|
| City | Chesterfield |
| State | MO |
| Event id | 98660 |
| Address 1 | 722 Goddard Ave |
| 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 |
| Postal code | 63005-1100 |
| Report date | 20260513 |
| Product type | Devices |
| Product quantity | 90 units |
| Reason for recall | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260325 |
| Initial firm notification | Letter |
| Center classification date | 20260506 |
Overview
- Recalling FirmKatalyst Surgical, LLC
- StatusOngoing
- Risk LevelClass II
- DistributionWorldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.