MITRACLIP SYSTEM STEERABLE GUIDE CATHETER Adverse Event — Malfunction (MDR 2024168-2020-03941)
MITRACLIP SYSTEM STEERABLE GUIDE CATHETER Adverse Event — Malfunction (MDR 2024168-2020-03941) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MITRACLIP SYSTEM STEERABLE GUIDE CATHETER; Generic name: VALVE REPAIR; Manufacturer: ABBOTT VASCULAR.
| Device | MITRACLIP SYSTEM STEERABLE GUIDE CATHETER |
|---|---|
| Generic name | VALVE REPAIR |
| Manufacturer | ABBOTT VASCULAR |
| Report number | 2024168-2020-03941 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | THE DEVICE IS EXPECTED TO BE RETURNED FOR INVESTIGATION. IT HAS NOT YET BEEN RECEIVED. A FOLLOW-UP REPORT WILL BE SUBMITTED WITH ALL ADDITIONAL RELEVANT INFORMATION. |
| Source | openFDA MAUDE (device adverse events) |
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