DEX Ophthalmic Tissue Forceps: recall status

⚠ Recalls found. DEX Ophthalmic Tissue Forceps is named in 12 official recalls in our current data:

FDA Class II recall Z-2069-2026 — Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
FDA Class II recall Z-2070-2026 — Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
FDA Class II recall Z-2071-2026 — Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
And 9 more listed below.

Brand: Katalyst Surgical

Recalls naming this model

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2069-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2070-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2071-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2072-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2073-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2074-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2075-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2076-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2077-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2078-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

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

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2079-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

DEX Ophthalmic Tissue Forceps recall — Katalyst Surgical, LLC

Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding…

Company / brand: Katalyst Surgical recalls

Affected product: DEX Ophthalmic Tissue Forceps recall status

Official ID Z-2080-2026 · Official record ↗

See all Katalyst Surgical recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.