FDA DevicesClass II
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog N...
Published: May 13, 2026Recall ID: Z-2069-2026Category: devicesCountry: US
Reason for Recall / Hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Product Description & Identification
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
Additional Source Details
| Field | Value |
|---|---|
| City | Chesterfield |
| State | MO |
| Event id | 98660 |
| Address 1 | 722 Goddard Ave |
| Code info | Lot Code: Model No: DVF4005-23 UDI-DI: (01)10817489021658(11)250924(17)280924(10)M50529 Lot Number: M50529 Expiration Date: 09/04/2028 |
| Postal code | 63005-1100 |
| Report date | 20260513 |
| Product type | Devices |
| Product quantity | 5 units |
| Reason for recall | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260325 |
| Initial firm notification | Letter |
| Center classification date | 20260506 |
Overview
- Recalling FirmKatalyst Surgical, LLC
- StatusOngoing
- Risk LevelClass II
- DistributionWorldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.