Warning
Katalyst Surgical Recalls DEX Ophthalmic Tissue Forceps
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #Z-2072-2026Medical Device
Katalyst Surgical Recalls DEX Ophthalmic Tissue Forceps
Katalyst Surgical, LLC · Class II — Moderate Risk
Product Description
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
Reason for Recall
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
Sources: FDA openFDA Enforcement Database