Reported May 13, 2026 · Ongoing
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-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 End Grasping Forceps
- Model/Catalog NumberDVF4022-25-S
- Lot codes and dates
11 of 11 products
Products covered by this recall Model / number Barcodes Product as published DVF4022-25-S10840096205142Lot Code: UDI-DI: (01)10840096205142(11)251125(17)281125(10)M51041 DVF4022-25-S10840096205142Lot Number: M51041 Expiration Date: 11/25/2028 UDI-DI: (01)10840096205142(11)250819(17)280819(10)M50093 DVF4022-25-S10840096205142Lot Number: M50093 Expiration Date: 08/19/2028 UDI-DI: (01)10840096205142(11)250924(17)280924(10)M50293 DVF4022-25-S10840096205142Lot Number: M50293 Expiration Date: 09/24/2028 UDI-DI: (01)10840096205142(11)250924(17)280924(10)M50216 DVF4022-25-S10840096205142Lot Number: M50216 Expiration Date: 09/24/2028 UDI-DI: (01)10840096205142(11)251021(17)281021(10)M50431 DVF4022-25-S10840096205142Lot Number: M50431 Expiration Date: 10/21/2028 UDI-DI: (01)10840096205142(11)251017(17)281017(10)M50543 DVF4022-25-S10840096205142Lot Number: M50543 Expiration Date: 10/17/2028 UDI-DI: (01)10840096205142(11)251023(17)281023(10)M50634 DVF4022-25-S10840096205142Lot Number: M50634 Expiration Date: 10/23/2028 UDI-DI: (01)10840096205142(11)251103(17)281103(10)M50903 DVF4022-25-S10840096205142Lot Number: M50903 Expiration Date: 11/03/2028 UDI-DI: (01)10840096205142(11)251113(17)281113(10)M50937 DVF4022-25-S10840096205142Lot Number: M50937 Expiration Date: 11/13/2028 UDI-DI: (01)10840096205142(11)251125(17)281125(10)M50997 — Lot Number: M50997 Expiration Date: 11/25/2028 - Amount recalled
- 235 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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