Reported May 13, 2026 · Ongoing
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
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, 23ga DEX NanoTapered AWH Forceps
- Model/Catalog NumberDVF4005-23
- Lot codes and dates
- Lot CodeModel
- NoDVF4005-23
- UDI-DI(01)10817489021658(11)250924(17)280924(10)M50529
- Lot NumberM50529
- Expiration Date09/04/2028
- Amount recalled
- 5 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.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Katalyst Surgical, LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.