FDA DeviceClass IINotable

FDA Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF40

Date: 2026-05-13
Brand: Katalyst Surgical, LLC
Category: Medical Device
FDA Class: Class II

Description

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Hazard

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Remedy

80 units

View original recall →
Share:

Related Recalls

2026-05-13 · FDA_DEVICE
FDA Recall: DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
Katalyst Surgical, LLC
2026-05-13 · FDA_DEVICE
FDA Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S
Katalyst Surgical, LLC
2026-05-13 · FDA_DEVICE
FDA Recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25
Katalyst Surgical, LLC
2026-05-13 · FDA_DEVICE
FDA Recall: DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
Katalyst Surgical, LLC