Home/Recalls/FDA-Z-2070-2026
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog ...

Published: May 13, 2026Recall ID: Z-2070-2026Category: 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 Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25

Additional Source Details

FieldValue
CityChesterfield
StateMO
Event id98660
Address 1722 Goddard Ave
Code infoLot Code: Model No: DVF4005-25 UDI-DI: (01)10817489021665(11)250924(17)280924(10)M50530 Lot Number: M50530 Expiration Date: 09/24/2028
Postal code63005-1100
Report date20260513
Product typeDevices
Product quantity10 units
Reason for recallField Safety Corrective Action for IFU in DEX Forceps and Scissors.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260325
Initial firm notificationLetter
Center classification date20260506

Overview

  • Recalling FirmKatalyst Surgical, LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Official Agency Alert