FDAFDA · Food and drugs·Recall number Z-2069-2026
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
Published May 13, 2026 · Recall initiated: March 25, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Katalyst Surgical, LLC
- Distributor
- Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.
- Lot
- Lot Code: Model No: DVF4005-23 UDI-DI: (01)10817489021658(11)250924(17)280924(10)M50529 Lot Number: M50529 Expiration Date: 09/04/2028
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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