Official recall notice
FDA DeviceClass IINotable
FDA Recall: DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27
- 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
150 units
Product description
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.