MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00240)
MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00240) 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 | 2023826-2008-00240 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, Distributor |
| Narrative | THE REPORTER STATED THE SURGEON ATTEMPTED TO INSERT AN EYEONICS LENS BUT THE TRAILING HAPTICS STRAIGHTENED OUT IN THE CARTRIDGE DURING ADVANCEMENT OF THE LENS. THERE WAS NO PT CONTACT. THE DOCTOR DECIDED TO USE A DIFFERENT LENS. THE REPORTER STATED IT WAS THE SURGEON'S OPINION THAT THE LIKELY CAUSE OF THE IOL DAMAGE WAS DUE TO THE MSI-TF INJECTOR. |
| Source | openFDA MAUDE (device adverse events) |
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