Official recall notice
FDA DeviceClass IINotable
FDA Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S
- 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
90 units
Product description
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.