CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING WITH DURAFLO TREATMENT Adverse Event — Death (MDR 6000002-2008-06073)
CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING WITH DURAFLO TREATMENT Adverse Event — Death (MDR 6000002-2008-06073) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING WITH DURAFLO TREATMENT; Generic name: ANNULOPLASTY RING; Manufacturer: ED
| Device | CARPENTIER-EDWARDS PHYSIO ANNULOPLASTY RING WITH DURAFLO TREATMENT |
|---|---|
| Generic name | ANNULOPLASTY RING |
| Manufacturer | EDWARDS LIFESCIENCES |
| Report number | 6000002-2008-06073 |
| 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 2 MONTHS PRIOR), DUE TO UNK REASONS. UNK IF PT DEATH IS DEVICE RELATED. |
| Source | openFDA MAUDE (device adverse events) |
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