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DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25

Class II
Recalling firm
Katalyst Surgical, LLC
Reason for recall
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Affected products (lot / model / serial)
Lot Code: Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250422(17)280422(10)M47116 Lot Number: M47116 Expiration Date: 04/22/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250610(17)280610(10)M48162 Lot Number: M48162 Expiration Date: 06/10/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250618(17)280618(10)M48276 Lot Number: M48276 Expiration Date: 06/18/2028 Model No: DVF4034-35 UDI-DI: (01)10817489025540(11)250626(17)280626(10)M48303 Lot Number: M48303 Expiration Date: 06/26/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250730(17)280730(10)M49168 Lot Number: M49168 Expiration Date: 07/30/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250807(17)280807(10)M49270 Lot Number: M49270 Expiration Date: 08/07/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250819(17)280819(10)M49285 Lot Number: M49285 Expiration Date: 08/19/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250819(17)280819(10)M49286 Lot Number: M49286 Expiration Date: 08/19/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250825(17)280825(10)M49775 Lot Number: M49775 Expiration Date: 08/25/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250825(17)280825(10)M49829 Lot Number: M49829 Expiration Date: 08/25/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250826(17)280826(10)M49905 Lot Number: M49905 Expiration Date: 08/26/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250917(17)280917(10)M50289 Lot Number: M50289 Expiration Date: 09/17/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250917(17)280917(10)M50208 Lot Number: M50208 Expiration Date: 09/17/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250924(17)280924(10)M50290 Lot Number: M50290 Expiration Date: 09/24/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251015(17)281015(10)M50916 Lot Number: M50916 Expiration Date: 10/15/2028 Model No:DVF4034-25 UDI-DI: (01)10817489025540(11)251020(17)281020(10)M50992 Lot Number: M50992 Expiration Date: 10/20/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251023(17)281023(10)M51033 Lot Number: M51033 Expiration Date: 10/23/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251029(17)281029(10)M51074 Lot Number: M51074 Expiration Date: 10/29/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251029(17)281029(10)M51075 Lot Number: M51075 Expiration Date: 10/29/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251113(17)281113(10)M51234 Lot Number: M51234 Expiration Date: 11/13/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251125(17)281125(10)M51290 Lot Number: M51290 Expiration Date: 11/25/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251126(17)281126(10)M51291 Lot Number: M51291 Expiration Date: 11/26/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)251209(17)281209(10)M51521 Lot Number: M51521 Expiration Date: 12/09/2028 Model No:DVF4034-25 UDI-DI: (01)10817489025540(11)251218(17)281218(10)M51628 Lot Number: M51628 Expiration Date: 12/18/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)260120(17)290120(1)M51698 Lot Number: M51698 Expiration Date: 01/20/2029 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)260203(17)290203(10)M51893 Lot Number: M51893 Expiration Date: 02/03/2029 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)260203(17)290203(10)M52019 Lot Number: M52019 Expiration Date: 02/03/2029
Units affected
750 units
Distribution pattern
Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Firm location
Chesterfield, MO, United States
Recall type
Voluntary: Firm initiated
How the firm notified customers
Letter
Product type
Devices
Status
Ongoing
Recall number
Z-2078-2026
Recall initiated
March 25, 2026
FDA classification date
May 6, 2026
FDA report date
May 13, 2026
FDA event ID
98660
Last updated on HTM Vibe
July 24, 2026
View on openFDA