Reported May 13, 2026 · Ongoing
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27
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, 27ga DEX Stiff Maculorhexis Forceps
- Model/Catalog NumberDVF4019-27
- Lot codes and dates
11 of 11 products
Products covered by this recall Model / number Barcodes Product as published DVF4019-2710817489022150Lot Code: UDI-DI: (01)10817489022150(11)251017(17)281017(10)M50931 DVF4019-2710817489022150Lot Number: M50931 Expiration Date: 10/17/2028 UDI-DI: (01)10817489022150(11)251209(17)281209(10)M51130 DVF4019-2710817489022150Lot Number: M51130 Expiration Date: 12/09/2028 UDI-DI: (01)10817489022150(11)260115(17)290115(10)M51589 DVF4019-2710817489022150Lot Number: M51589 Expiration Date: 01/15/2029 UDI-DI: (01)10817489022150(11)260205(17)290205(10)M52018 DVF4019-2710817489022150Lot Number: M52018 Expiration Date: 02/05/2029 UDI-DI: (01)10817489022150(11)260220(17)290220(10)M52195 DVF4019-2710817489022150Lot Number: M52195 Expiration Date: 2/20/2029 UDI-DI: (01)10817489022150(11)250909(17)280909(10)M50073 DVF4019-2710817489022150Lot Number: M50073 Expiration Date: 09/09/2028 UDI-DI: (01)10817489022150(11)250909(17)280909(10)M50287 DVF4019-2710817489022150Lot Number: M50287 Expiration Date: 09/09/2028 UDI-DI: (01)10817489022150(11)251007(17)281007(10)M50677 DVF4019-2710817489022150Lot Number: M50677 Expiration Date: 10/07/2028 UDI-DI: (01)10817489022150(11)251103(17)281103(0)M50991 DVF4019-2710817489022150Lot Number: M50991 Expiration Date: 11/03/2028 UDI-DI: (01)10817489022150(11)251113(17)281113(10)M51071 — Lot Number: M51071 Expiration Date: 11/13/2028 - Amount recalled
- 150 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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