FDAFDA · Food and drugs·Recall number Z-2079-2026
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
Published May 13, 2026 · Recall initiated: March 25, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Katalyst Surgical, LLC
- Distributor
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
- Lot
- Lot Code: Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)250429(17)280429(10)M47337 Lot Number: M47337 Expiration Date: 04/29/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251023(17)281023(10)M50921 Lot Number: M50921 Expiration Date: 10/23/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51525 Lot Number: M51525 Expiration Date: 12/09/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51526 Lot Number: M51526 Expiration Date: 12/09/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)260220(17)290220(10)M52172 Lot Number: M52172 Expiration Date: 02/20/2029
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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