ACRYSOF TORIC Adverse Event — Malfunction (MDR 1119421-2008-00082)
ACRYSOF TORIC Adverse Event — Malfunction (MDR 1119421-2008-00082) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACRYSOF TORIC; Generic name: INTRAOCULAR LENS; Manufacturer: ALCON RESEARCH, LTD. / HUNTINGTON.
| Device | ACRYSOF TORIC |
|---|---|
| Generic name | INTRAOCULAR LENS |
| Manufacturer | ALCON RESEARCH, LTD. / HUNTINGTON |
| Report number | 1119421-2008-00082 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | User facility |
| Narrative | FACILITY REPORTED A CRACKED LENS. ADDITIONAL INFORMATION HAS BEEN REQUESTED. |
| Source | openFDA MAUDE (device adverse events) |
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