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Ophthalmic Forceps recalls

The FDA has posted 13 enforcement recalls of ophthalmic forceps devices since 2025, none of them Class I (most serious). Most recent report: May 13, 2026.

Class II: 13

Who is recalling these devices

Latest recalls

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Class IIOngoingZ-2080-2026

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps

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

  • Ophthalmic Forceps
  • Under Investigation by firm
Katalyst Surgical, LLCMOMay 13, 2026

Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Forceps, Ophthalmic”). Informational only — verify against the FDA before acting.