FDA recall Z-2069-2026

Katalyst Surgical, LLC · Class II · device

Product

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

Reason for recall

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

Distribution

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

Key facts

Status
Ongoing
Initiation date
2026-03-25
Report date
2026-05-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Chesterfield, MO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2069-2026