MICRO DRIVER RX CORONARY STENT SYSTEM Adverse Event — Injury (MDR 2953200-2008-00067)
MICRO DRIVER RX CORONARY STENT SYSTEM Adverse Event — Injury (MDR 2953200-2008-00067) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICRO DRIVER RX CORONARY STENT SYSTEM; Manufacturer: MEDTRONIC IRELAND; Report number: 2953200-2008-00067.
| Device | MICRO DRIVER RX CORONARY STENT SYSTEM |
|---|---|
| Manufacturer | MEDTRONIC IRELAND |
| Report number | 2953200-2008-00067 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-20 |
| Report source | Health Professional, Company representation |
| Narrative | A 2.75MM DIAMETER X 12MM LENGTH MICRO DRIVER RX CORONARY STENT SYSTEM WAS INSERTED INTO A PT FOR THE TREATMENT OF A MID LEFT CIRCUMFLEX. THE VESSEL MORPHOLOGY IS UNK. IT WAS REPORTED THAT THE PHYSICIAN HAD IMPLANTED A DRV27512X IN THE LEFT CIRCUMFLEX LESION. THE PHYSICIAN THEN ATTEMPTED TO PASS THE FIRST STENT, THE STENT WAS PULLED OFF THE BALLOON. THE PHYSICIAN STATED THAT THE STENT MUST HAVE CAU |
| Source | openFDA MAUDE (device adverse events) |
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