NOVASURE IMPEDANCE CONTROLLED EA SYSTEM
Report
- Report Number
- 1222780-2010-00198
- Event Type
- Injury
- Date Received
- December 10, 2010
- Date of Event
- November 2, 2010
- Report Date
- November 12, 2010
- Manufacturer
- HOLOGIC
- Product Code
- MNB
- PMA / PMN Number
- P010013
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- PHYSICIAN
Narratives
LOT AND SERIAL NUMBER OF THE DISPOSABLE DEVICE NOT PROVIDED BY THE COMPLAINANT, THEREFORE, THE EXPIRATION DATE IS NOT KNOWN. THE DEVICE IS NOT BEING RETURNED, THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE CAN NOT BE COMPLETED. LOT NUMBER NOT PROVIDED BY THE COMPLAINANT, THEREFORE, THE MANUFACTURE DATE IS NOT KNOWN. BASED ON THE INFORMATION OBTAINED TO DATE, NO DIRECT CORRELATION CAN BE MADE BETWEEN THE REPORTED EVENT AND THE NOVASURE SYSTEM. IF ADDITIONAL RELEVANT INFORMATION IS REC'D, A SUPPLEMENTAL MEDWATCH WILL BE FILED. DEVICE HISTORY RECORD (DHR) REVIEW COULD NOT BE CONDUCTED FOR THE DISPOSABLE DEVICE AS A LOT AND SERIAL NUMBER WERE NOT PROVIDED BY THE COMPLAINANT. (B)(4).
IT WAS REPORTED THAT AN UNEVENTFUL NOVASURE ENDOMETRIAL ABLATION TOOK PLACE ON (B)(6)2010 FOLLOWED BY A "PELVIC INFECTION". ON (B)(6) 2010, THE PT PRESENTED WITH PELVIC PAIN AND VAGINAL DISCHARGE. SHE WAS ADMITTED TO THE HOSPITAL AND LAB WORK AND AN ULTRASOUND WERE PERFORMED WITH FINDINGS OF (B)(6). THE PT WAS TREATED WITH ANTIBIOTICS AND DISCHARGED ON (B)(6) 2010. ON (B)(6) 2010, IT WAS REPORTED THE PT WAS SEEN ON F/U AND WAS "BETTER". WE HAVE BEEN UNABLE TO OBTAIN ADDITIONAL INFORMATION SURROUNDING THE PELVIC INFECTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NOVASURE IMPEDANCE CONTROLLED EA SYSTEM | MNB | HOLOGIC | NS2000 | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 31 YR | Other | RADIO FREQUENCY CONTROLLER - SERIAL # UNK |