Recall
FDAHealthMarch 25, 2026

Katalyst Surgical, LLC — DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 25, 2026

Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.

What's affected?

Product
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
Lot code
Model

Additional details

Lot Code: Model No: DVF4005-23 UDI-DI: (01)10817489021658(11)250924(17)280924(10)M50529 Lot Number: M50529 Expiration Date: 09/04/2028

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 5 units.

View original FDA notice →

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