Recall Z-2077-2026— Katalyst Surgical, LLC
Class II · Ongoing
Class II FDA medical device recall by Katalyst Surgical, LLC, initiated 2026-03-25. FDA's recall record names no specific 510(k) clearance for this event. Product: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S. Reason: Field Safety Corrective Action for IFU in DEX Forceps and Scissors..
- Recalling firm
- Katalyst Surgical, LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-03-25
- Firm location
- Chesterfield, MO, United States
Product description
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S
Reason for recall
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Data sourced from openFDA. This site is unofficial and independent of the FDA.