Class II U.S. Food and Drug Administration

Katalyst Surgical, LLC DEX Ophthalmic Tissue Forceps recall: Field Safety Corrective Action for IFU in DEX Forceps and Scissors

Recall published 6 months ago

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

The hazard: Device safety concern

This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

What the notice says: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-2076-2026
Published
May 13, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Katalyst Surgical, LLC
Product type
Medical devices
Units affected
150 units
Distribution
Nationwide
Made in
United States
Lot / code info
Lot Code: Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)251017(17)281017(10)M50931 Lot Number: M50931 Expiration Date: 10/17/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)251209(17)281209(10)M51130 Lot Number: M51130 Expiration Date: 12/09/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)260115(17)290115(10)M51589 Lot Number: M51589 Expiration Date: 01/15/2029 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)260205(17)290205(10)M52018 Lot Number: M52018 Expiration Date: 02/05/2029 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)260220(17)290220(10)M52195 Lot Number: M52195 Expiration Date: 2/20/2029 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)250909(17)280909(10)M50073 Lot Number: M50073 Expiration Date: 09/09/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)250909(17)280909(10)M50287 Lot Number: M50287 Expiration Date: 09/09/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)251007(17)281007(10)M50677 Lot Number: M50677 Expiration Date: 10/07/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)251103(17)281103(0)M50991 Lot Number: M50991 Expiration Date: 11/03/2028 Model No: DVF4019-27 UDI-DI: (01)10817489022150(11)251113(17)281113(10)M51071 Lot Number: M51071 Expiration Date: 11/13/2028
UPC codes
10817489022150

Products covered by this recall

DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27

Check your product

The notice names 16 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 10817489022150

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • 10
  • 17
  • 12
  • 09
  • 01
  • 15
  • 02
  • 05
  • 20
  • 07
  • 11
  • 03
  • 13
  • 2028 — 150 units

Model or item number

On the rating label, the box or the instruction sheet.

  • DVF4019-27 UDI-DI

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Katalyst Surgical, LLC — This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Replacements, repairs and reimbursement

Device remedies run through the supply chain, so the route depends on who sold you the unit.

  • Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.
  • If the device was billed to insurance or Medicare, the replacement is usually billed the same way; you should not face a second deductible for a recall.
  • Keep every piece of correspondence. If a recalled device caused harm, that paper trail is what a claim rests on.
  • Consumer-purchased devices such as monitors and test kits are normally replaced free, with return shipping paid.

Company contact: Katalyst Surgical, LLC — 722 Goddard Ave, Chesterfield, MO, 63005-1100

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Katalyst Surgical, LLC medical devices recalled?

Field Safety Corrective Action for IFU in DEX Forceps and Scissors. Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 10817489022150; best-by date 10 or 17; model number DVF4019-27 UDI-DI. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.

Where was the recalled product sold?

It was distributed nationwide.

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