MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00232)
MICROSTAAR INJECTOR Adverse Event — Malfunction (MDR 2023826-2008-00232) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICROSTAAR INJECTOR; Generic name: INTRAOCULAR LENS GUIDE; Manufacturer: STAAR SURGICAL CO..
| Device | MICROSTAAR INJECTOR |
|---|---|
| Generic name | INTRAOCULAR LENS GUIDE |
| Manufacturer | STAAR SURGICAL CO. |
| Report number | 2023826-2008-00232 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Other |
| Narrative | THE REPORTER STATED A 3.0 DIOPTER AQ5010V SILICONE THREE PIECE LENS WAS TORN UPON INJECTION DUE TO A FAULTY INJECTOR. THERE WAS NO PT CONTACT. ADD'L INFO HAS BEEN REQUESTED BUT NONE HAS BEEN FORTHCOMING. IF ADD'L INFO BECOMES AVAILABLE, A SUPPLEMENTAL MEDWATCH WILL BE SENT. |
| Source | openFDA MAUDE (device adverse events) |
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