ESSURE Adverse Event — Injury (MDR 2951250-2020-05870)
ESSURE Adverse Event — Injury (MDR 2951250-2020-05870) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ESSURE; Generic name: TRANSCERVICAL CONTRACEPTIVE TUBAL OCCLUSION DEVICE; Manufacturer: BAYER PHARMA AG.
| Device | ESSURE |
|---|---|
| Generic name | TRANSCERVICAL CONTRACEPTIVE TUBAL OCCLUSION DEVICE |
| Manufacturer | BAYER PHARMA AG |
| Report number | 2951250-2020-05870 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | THIS SPONTANEOUS CASE WAS REPORTED BY A LAWYER AND DESCRIBES THE OCCURRENCE OF ECTOPIC PREGNANCY WITH CONTRACEPTIVE DEVICE ('FOUND DEAD FETUS ATTACHED UNDER TUBES'), MEDICAL DEVICE REMOVAL ('HAD MY TUBES REMOVED AND SOME FIBROIDS TAKEN OUT') AND MYOMECTOMY ('HAD MY TUBES REMOVED AND SOME FIBROIDS TAKEN OUT') IN A FEMALE PATIENT WHO HAD ESSURE INSERTED. THE OCCURRENCE OF ADDITIONAL NON-SERIOUS EVEN |
| Source | openFDA MAUDE (device adverse events) |
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