FDA Adverse Event
Injury
Summary report: N
ARIS TRANS-OBTURATOR
MDR report key: 3842728
·
Received January 24, 2014
Report
- Report Number
- 2125050-2014-00087
- Event Type
- Injury
- Date Received
- January 24, 2014
- Date of Event
- January 14, 2009
- Report Date
- January 23, 2014
- Manufacturer
- COLOPLAST A/S
- Product Code
- FTL
- PMA / PMN Number
- K050148
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- ATTORNEY
Narratives
Additional Manufacturer Narrative · 1
COLOPLAST HAS NOT BEEN PROVIDED ANY CORROBORATING EVIDENCE TO VERIFY THE INFORMATION CONTAINED IN THIS REPORT.
Description of Event or Problem · 1
AS REPORT TO COLOPLAST THOUGH NOT VERIFIED, PT WAS IMPLANTED WITH ARIS AND NOVASILK MESH. LATER THE PT EXPERIENCE PAIN, BLEEDING, DYSPAREUNIA AND MESH EROSION. EXCISIONS OF THE MESH, REVISION OF VAGINAL WALL INCISION AND CYSTOSCOPY WERE PERFORMED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 55810 | ARIS TRANS-OBTURATOR | POLYMERIC SUGICAL MESH | FTL | COLOPLAST A/S | 5195501000 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |