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Recall Observatory FDA recall evidence

Device product

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

Z-2069-2026

March 25, 2026

Class II

Product summary

Firm
Katalyst Surgical, LLC
Event
Event 98660
Status
Ongoing
Classification
Class II
Quantity
5 units
Official record key
device-enforcement:Z-2069-2026

Official wording

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

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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