MICROSTAAR INJECTOR CARTRIDGE Adverse Event — Malfunction (MDR 2023826-2008-00238)
MICROSTAAR INJECTOR CARTRIDGE Adverse Event — Malfunction (MDR 2023826-2008-00238) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICROSTAAR INJECTOR CARTRIDGE; Generic name: INTRAOCULAR LENS GUIDE; Manufacturer: STAAR SURGICAL CO..
| Device | MICROSTAAR INJECTOR CARTRIDGE |
|---|---|
| Generic name | INTRAOCULAR LENS GUIDE |
| Manufacturer | STAAR SURGICAL CO. |
| Report number | 2023826-2008-00238 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Other, Company representation |
| Narrative | THE REPORTER STATED AN AQ CARTRIDGE-FP CARTRIDGE POUCH WAS OPENED AND IT WAS NOTED THERE WAS MOISTURE IN THE POUCH AND THE CARTRIDGE WAS WET. THE PROD WAS NOT USED AND THERE WAS NO PT CONTACT. |
| Source | openFDA MAUDE (device adverse events) |
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