FDA DeviceClass IINotable
FDA Recall: DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23
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
50 units
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