MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM Adverse Event — Malfunction (MDR 2024168-2008-00114)
MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM Adverse Event — Malfunction (MDR 2024168-2008-00114) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM; Generic name: 74MAF; Manufacturer: ABBOTT VASCULAR-CARDIAC THERAPIES.
| Device | MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM |
|---|---|
| Generic name | 74MAF |
| Manufacturer | ABBOTT VASCULAR-CARDIAC THERAPIES |
| Report number | 2024168-2008-00114 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-14 |
| Report source | Foreign, Health Professional, Distributor |
| Narrative | REPORTING RATIONALE: MALFUNCTION. REPORTING STATUS: STENT DISLODGEMENT HAS CAUSED OR CONTRIBUTED TO PATIENT INJURY PREVIOUSLY. DEVICE ISSUE: STENT DISLODGEMENT. IT WAS REPORTED THAT THE STENT DID NOT CROSS. NO ADDITIONAL EVENT OR PATIENT INFORMATION IS AVAILABLE. THE EVENT IS BEING REPORTED BASED ON THE RETURNED DEVICE ANALYSIS WHICH REVEALED THAT THE STENT WAS PARTIALLY DISLODGED FROM THE BALLOON |
| Source | openFDA MAUDE (device adverse events) |
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