Official recall notice
FDA DeviceClass IINotable
FDA Recall: DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
- Recall date
- 2026-05-13
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Recommended action
What to do
5 units
Product description
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.