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Home › FDA recalls › DEX Ophthalmic Tissue Forceps
CLASS II · ModerateFDA

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

📅 Mar 25, 2026 · 📍 Nationwide
Recalling company
Katalyst Surgical, LLC
Product
DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25
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
750 units
Lot / codes
Lot Code: Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250422(17)280422(10)M47116 Lot Number: M47116 Expiration Date: 04/22/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250610(17)280610(10)M48162 Lot Number: M48162 Expiration Date: 06/10/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250618(17)280618(10)M48276 Lot Number: M48276 Expiration Date: 06/18/2028 Model No: DVF4034-35 UDI-DI: (01)10817489025540(11)250626(17)280626(10)M48303 Lot Number: M48303 Expiration Date: 06/26/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250730(17)280730(10)M49168 Lot Number: M49168 Expiration Date: 07/30/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250807(17)280807(10)M49270 Lot Number: M49270 Expiration Date: 08/07/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250819(17)280819(10)M49285 Lot Number: M49285 Expiration Date: 08/19/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250819(17)280819(10)M49286 Lot Number: M49286 Expiration Date: 08/19/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250825(17)280825(10)M49775 Lot Number: M49775 Expiration Date: 08/25/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250825(17)280825(10)M49829 Lot Number: M49829 Expiration Date: 08/25/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250826(17)280826(10)M49905 Lot Number: M49905 Expiration Date: 08/26/2028 Model No: DVF4034-25 UDI-DI: (01)10817489025540(11)250917(17)280917(10)M50289 Lot Number: M50289 Expirat
Company location
Chesterfield, MO
Recall type
Voluntary: Firm initiated
Recall number
Z-2078-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2078-2026 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.