ACRYSOF IQ RESTOR MULTIFOCAL LENS Adverse Event — Malfunction (MDR MW5094271)
ACRYSOF IQ RESTOR MULTIFOCAL LENS Adverse Event — Malfunction (MDR MW5094271) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACRYSOF IQ RESTOR MULTIFOCAL LENS; Generic name: LENS, MULTIFOCAL INTRAOCULAR; Manufacturer: ALCON RESEARCH, LLC.
| Device | ACRYSOF IQ RESTOR MULTIFOCAL LENS |
|---|---|
| Generic name | LENS, MULTIFOCAL INTRAOCULAR |
| Manufacturer | ALCON RESEARCH, LLC |
| Report number | MW5094271 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-24 |
| Narrative | VISION DISTURBANCES; HAD ACRYSOF IQ RESTOR LENS IMPLANTED IN BOTH EYES. HAD HALO TYPE VISION DISTURBANCES IMMEDIATELY (WHICH IS COMMON) BUT STILL HAVE THE SAME TO THIS DAY. HAD ANOTHER PROCEDURE DONE CALLED YAG CAPSULOTOMY AND NOW HAVE STREAKS AT NIGHT IN THE VISION FOR BOTH EYES. FDA SAFETY REPORT ID# (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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