Reported May 13, 2026 · Ongoing

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-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 Asymmetrical Tano Forceps
  • Model/Catalog NumberDVF4014-25-S
Lot codes and dates

5 of 5 products

Products covered by this recall
Model / numberBarcodesProduct as published
DVF4014-25-S10840096205111Lot Code: UDI-DI: (01)10840096205111(11)250909(17)280909(10)M49277
DVF4014-25-S10840096205111Lot Number: M49277 Expiration Date: 09/09/2028 UDI-DI: (01)10840096205111(11)250513(17)280513(10)M47588
DVF4014-25-S10840096205111Lot Number: M47588 Expiration Date: 05/13/2028 UDI-DI: (01)10840096205111(11)250506(17)280506(10)M47364
DVF4014-25-S10840096205111Lot Number: M47364 Expiration Date: 05/06/2028 UDI-DI: (01)10840096205111(11)250506(17)280506(10)M47363
Lot Number: M47363 Expiration Date: 05/06/2028
Amount recalled
80 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:38 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.