MICROSTAAR INJECTOR Adverse Event — Injury (MDR 2023826-2008-00243)
MICROSTAAR INJECTOR Adverse Event — Injury (MDR 2023826-2008-00243) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICROSTAAR INJECTOR; Generic name: INTRAOCULAR LENS FOLDERS AND INJECTORS; Manufacturer: STAAR SURGICAL CO..
| Device | MICROSTAAR INJECTOR |
|---|---|
| Generic name | INTRAOCULAR LENS FOLDERS AND INJECTORS |
| Manufacturer | STAAR SURGICAL CO. |
| Report number | 2023826-2008-00243 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, Distributor |
| Narrative | THE REPORTER STATED THE SURGEON INSERTED AN EYEONICS LENS BUT THE HAPTIC BROKE. THE INCISION WAS ENLARGED TO REMOVE THE LENS AND ANOTHER SAME TYPE LENS WAS IMPLANTED. SUTURES WERE REQUIRED TO CLOSE THE INCISION. THE CAUSE OF THE IOL DAMAGE MAY HAVE BEEN DUE TO THE MSI-TF INJECTOR. |
| Source | openFDA MAUDE (device adverse events) |
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