ESSURE Adverse Event — Injury (MDR 2951250-2020-05937)
ESSURE Adverse Event — Injury (MDR 2951250-2020-05937) 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 | 2951250-2020-05937 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | THIS SPONTANEOUS CASE WAS REPORTED BY A LAWYER AND DESCRIBES THE OCCURRENCE OF DEVICE BREAKAGE ('BROKEN PIECE OF METAL THAT CAME OUT AND LODGE ITSELF IN MY OVARY'), EMBEDDED DEVICE ('MY MIGRATED COIL WAS EMBEDDED IN MY OMENTUM OF MY INTESTINE AND PARTIALLY TO THE OUT SIDE OF MY FALLOPIAN TUBE/BROKEN PIECE OF METAL THAT CAME OUT AND LODGE ITSELF IN MY OVAR') AND DEVICE DISLOCATION ('MY MIGRATED COI |
| Source | openFDA MAUDE (device adverse events) |
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