CARPENTIER-EDWARDS CLASSIC ANNULOPLASTY RING Adverse Event — Death (MDR 6000002-2008-06074)
CARPENTIER-EDWARDS CLASSIC ANNULOPLASTY RING Adverse Event — Death (MDR 6000002-2008-06074) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CARPENTIER-EDWARDS CLASSIC ANNULOPLASTY RING; Generic name: ANNULOPLASTY RING; Manufacturer: EDWARDS LIFESCIENCES.
| Device | CARPENTIER-EDWARDS CLASSIC ANNULOPLASTY RING |
|---|---|
| Generic name | ANNULOPLASTY RING |
| Manufacturer | EDWARDS LIFESCIENCES |
| Report number | 6000002-2008-06074 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-18 |
| Report source | Foreign, Health Professional, User facility |
| Narrative | REPORTEDLY, PT EXPIRED APPROX AFTER AN IMPLANT DURATION OF 2.13 MONTHS (IN 2007, AFTER AN IMPLANT DATE OF APPROX TWO MONTHS EARLIER), DUE TO UNK REASONS. UNK IF PT DEATH IS DEVICE RELATED. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →