Home/Recalls/FDA-Z-2073-2026
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Numb...

Published: May 13, 2026Recall ID: Z-2073-2026Category: devicesCountry: US

Reason for Recall / Hazard

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Product Description & Identification

DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23

Additional Source Details

FieldValue
CityChesterfield
StateMO
Event id98660
Address 1722 Goddard Ave
Code infoLot Code: Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)250807(17)280807(10)M49267 Lot Number: M49267 Expiration Date: 08/07/2028 Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)251017(17)281017(10)M50930 Lot Number: M50930 Expiration Date: 10/17/2028 Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)251113(17)281113(10)M51230 Lot Number: M51230 Expiration Date: 11/13/2028 Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)251212(17)281212(10)M51587 Lot Number: M51587 Expiration Date: 12/12/2028 Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)260115(17)290115(10)M51696 Lot Number: M51696 Expiration Date: 01/15/2029 Model No: DVF4019-23 UDI-DI: (01)10817489022136(11)250904(17)280904(10)M49921 Lot Number: M49921 Expiration Date: 09/04/2028 Model No; DVF4019-23 UDI-DI: (01)10817489022136(11)251107(17)281107(10)M51128 Lot Number: M51128 Expiration Date: 11/07/2028
Postal code63005-1100
Report date20260513
Product typeDevices
Product quantity50 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