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Source: FDA | Recall date: 05/13/2026
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Affected product: DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
Summary: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Hazard: Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Track your baby products and get automatic recall alerts when something may affect your family.
Learn more about the baby product recall tracker, baby product recall alerts, or recall monitoring plans.