Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
- Recall date
- March 25, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2079-2026
- FDA classification
- Class II
- Brand / firm
- Katalyst Surgical, LLC
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
Why it was recalled
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
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