MULTI-LINK RX VISION CORONARY STENT SYSTEM Adverse Event — Malfunction (MDR 2024168-2008-00104)
MULTI-LINK RX VISION CORONARY STENT SYSTEM Adverse Event — Malfunction (MDR 2024168-2008-00104) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MULTI-LINK RX VISION CORONARY STENT SYSTEM; Generic name: 74MAF; Manufacturer: ABBOTT VASCULAR-CARDIAC THERAPIES.
| Device | MULTI-LINK RX VISION CORONARY STENT SYSTEM |
|---|---|
| Generic name | 74MAF |
| Manufacturer | ABBOTT VASCULAR-CARDIAC THERAPIES |
| Report number | 2024168-2008-00104 |
| Event type | Malfunction |
| Product problem | N |
| Date received | 2008-02-14 |
| Report source | Foreign, Company representation |
| Narrative | REPORTING STATUS: SERIOUS INJURY/ MEDICAL INTERVENTION. REPORTING RATIONALE: DISSECTION REQUIRING MEDICAL INTERVENTION. DEVICE ISSUE: NONE. IT WAS REPORTED THAT WHILE IMPLANTING THE MULTI LINK VISION STENT, THE PROXIMAL EDGE OF THE STENT CAUSED A DISSECTION OF THE RCA VESSEL. A 3.5 X 13 MM MULTI-LINK ZETA STENT WAS USED TO TREAT THE DISSECTION. NO ADDITIONAL EVENT OR PT INFO IS AVAILABLE. |
| Source | openFDA MAUDE (device adverse events) |
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