MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00241)
MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00241) 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 | 2023826-2008-00241 |
| Event type | Malfunction |
| 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 LENS TORE. THE LENS WAS REMOVED WITH NO PT INJURY. THE REPORTER STATED IT WAS THE SURGEON'S OPINION THAT THE LIKELY CAUSE OF THE IOL DAMAGE WAS DUE TO THE MSI-PF INJECTOR AND THE FOAM TIP PLUNGER. |
| Source | openFDA MAUDE (device adverse events) |
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