LADARVISION 4000 Adverse Event — Malfunction (MDR 1061857-2008-00012)
LADARVISION 4000 Adverse Event — Malfunction (MDR 1061857-2008-00012) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LADARVISION 4000; Generic name: OPHTHALMIC EXCIMER LASER SYSTEM; Manufacturer: ALCON - ORLANDO TECHNOLOGY CENTER.
| Device | LADARVISION 4000 |
|---|---|
| Generic name | OPHTHALMIC EXCIMER LASER SYSTEM |
| Manufacturer | ALCON - ORLANDO TECHNOLOGY CENTER |
| Report number | 1061857-2008-00012 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | A SYSTEM OPERATOR REPORTS, THE SYSTEM STOPPED TRACKING AT 85% INTO A PROCEDURE. AFTER SEVERAL ATTEMPTS, THEY WERE ABLE TO REACQUIRE AND COMPLETE THE SURGERY. FOLLOW-UP INFO FROM THE SITE INDICATES THIS PT WAS NOT HARMED/INJURED BY THIS EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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