Reported May 13, 2026 · Ongoing
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
Katalyst Surgical, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Katalyst Surgical, LLC · 722 Goddard Ave · Chesterfield, MO · 63005-1100
Is this the product you have?
- DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps
- Model/Catalog NumberDVF4034-25-S
- Lot codes and dates
6 of 6 products
Products covered by this recall Model / number Barcodes Product as published DVF4034-25-S10840096205166Lot Code: UDI-DI: (01)10840096205166(11)250429(17)280429(10)M47337 DVF4034-25-S10840096205166Lot Number: M47337 Expiration Date: 04/29/2028 UDI-DI: (01)10840096205166(11)251023(17)281023(10)M50921 DVF4034-25-S10840096205166Lot Number: M50921 Expiration Date: 10/23/2028 UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51525 DVF4034-25-S10840096205166Lot Number: M51525 Expiration Date: 12/09/2028 UDI-DI: (01)10840096205166(11)251209(17)281209(10)M51526 DVF4034-25-S10840096205166Lot Number: M51526 Expiration Date: 12/09/2028 UDI-DI: (01)10840096205166(11)260220(17)290220(10)M52172 — Lot Number: M52172 Expiration Date: 02/20/2029 - Amount recalled
- 50 units
This recall covers 12 products
The agency filed one notice per product. You are reading one of them; the other 11 are below.
Where it was sold
- Nationwide
Why it was recalled
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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