INTRAOCULAR LENS Adverse Event — Malfunction (MDR 2023826-2008-00225)
INTRAOCULAR LENS Adverse Event — Malfunction (MDR 2023826-2008-00225) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTRAOCULAR LENS; Generic name: INTRAOCULAR LENS; Manufacturer: STAAR SURGICAL CO..
| Device | INTRAOCULAR LENS |
|---|---|
| Generic name | INTRAOCULAR LENS |
| Manufacturer | STAAR SURGICAL CO. |
| Report number | 2023826-2008-00225 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional |
| Narrative | THE REPORTER STATED THAT THE SURGEON WAS INSERTING A IMPLANTABLE COLLAMER LENS MODEL MICL 12.6 AND THE LENS TORE. THE SURGEON REMOVED THE LENS WITH NO PT INJURY AND INSERTED THE BACK UP LENS. |
| Source | openFDA MAUDE (device adverse events) |
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