Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2073-2026 — DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23

U.S. FDA — Device Enforcement · United States · 2026-03-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2073-2026
Date of alert
2026-03-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Katalyst Surgical, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10817489022136
Reported risk: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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