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INFINITI VISION SYSTEM Adverse Event — Malfunction (MDR 2028159-2008-00063)

INFINITI VISION SYSTEM Adverse Event — Malfunction (MDR 2028159-2008-00063) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INFINITI VISION SYSTEM; Generic name: OPHTHALMIC SURGERY SYSTEM; Manufacturer: ALCON - IRVINE TECH CTR.

DeviceINFINITI VISION SYSTEM
Generic nameOPHTHALMIC SURGERY SYSTEM
ManufacturerALCON - IRVINE TECH CTR
Report number2028159-2008-00063
Event typeMalfunction
Product problemY
Date received2008-02-15
Report sourceHealth Professional, Company representation
NarrativeTHE CUSTOMER REPORTED AN ERROR MESSAGED DISPLAYED DURING SET UP. THERE WERE FOUR CASES CANCELLED. NO PT INJURY WAS REPORTED. MULTIPLE ATTEMPTS WERE MADE FOR PT STATUS WITH NO RESPONSE.
SourceopenFDA MAUDE (device adverse events)

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