Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps
- Recalling company
- Katalyst Surgical, LLC
- Product
- DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
- Reason
- Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 25, 2026
- Reported
- May 13, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
- Status
- Ongoing
- Quantity
- 50 units
- Lot / codes
- Lot Code: Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)250429(17)280429(10)M47337 Lot Number: M47337 Expiration Date: 04/29/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251023(17)281023(10)M50921 Lot Number: M50921 Expiration Date: 10/23/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51525 Lot Number: M51525 Expiration Date: 12/09/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51526 Lot Number: M51526 Expiration Date: 12/09/2028 Model No: DVF4034-25-S UDI-DI: (01)10840096205166(11)260220(17)290220(10)M52172 Lot Number: M52172 Expiration Date: 02/20/2029
- Company location
- Chesterfield, MO
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2079-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2079-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.