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TECNIS CL Adverse Event — Malfunction (MDR 2648035-2020-00396)

TECNIS CL Adverse Event — Malfunction (MDR 2648035-2020-00396) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TECNIS CL; Generic name: MONOFOCAL IOLS; Manufacturer: JOHNSON & JOHNSON SURGICAL VISION, INC..

DeviceTECNIS CL
Generic nameMONOFOCAL IOLS
ManufacturerJOHNSON & JOHNSON SURGICAL VISION, INC.
Report number2648035-2020-00396
Event typeMalfunction
Product problemY
Date received2020-04-27
NarrativeADDITIONAL INFORMATION: FROM THE 79 EVENTS: CARTRIDGE CRACK, LENS DAMAGED ¿ 4, CARTRIDGE DAMAGED, DIFFICULT TO USE, LENS DAMAGED ¿ 6, CARTRIDGE DAMAGED, DIFFICULT TO USE, LENS DAMAGED, OVERRIDE ¿ 1, CARTRIDGE DAMAGED, HAPTIC DAMAGED ¿ 1, CARTRIDGE DAMAGED, IOL TORN, LENS DAMAGED ¿ 1, CARTRIDGE DAMAGED, LENS DAMAGED ¿ 1, CARTRIDGE TIP CRACKED/ DAMAGED, HAPTIC DAMAGED, OVERRIDE ¿ 2, COSMETIC ISSUES
SourceopenFDA MAUDE (device adverse events)

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