Class II

Medical Device Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S

Katalyst Surgical, LLC · March 25, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

235 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2077-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Katalyst Surgical, LLC Medical Device Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S | SafeCheck