PROLIFT PELVIC FLOOR REPAIR
Report
- Report Number
- 2210968-2013-01197
- Event Type
- Injury
- Date Received
- February 15, 2013
- Report Date
- January 23, 2013
- Manufacturer
- ETHICON INC
- Product Code
- OTP
- PMA / PMN Number
- K013718
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- ATTORNEY
Narratives
(B)(4): NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY.IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIATHIS IS ONE OF TWO MEDWATCHES BEING SUBMITTED AS TWO DEVICES WERE INVOLVED IN THIS EVENT. SEE ALSO MEDWATCH 2210968-2013-01195. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.
IT WAS REPORTED THAT THE PATIENT UNDERWENT VAGINAL MESH REMOVAL/REVISION AND A CYSTOSCOPY ON (B)(6) 2012 BY DR. (B)(6), DUE TO VAGINAL MESH EXPOSURE/EROSION.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND A MESH WAS IMPLANTED. THE PATIENT EXPERIENCED PAIN, MESH EROSION, INFECTION, BLEEDING, VAGINAL SCARRING/SHRINKAGE AND EXPOSURE/EXTRUSION/PROTRUSION, THE PATIENT HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION IS PROVIDED AT THIS TIME.
IT WAS REPORTED THAT THE PATIENT UNDERWENT VAGINAL MESH REMOVAL/REVISION AND A CYSTOSCOPY ON (B)(6) 2012 BY DR. (B)(6), DUE TO VAGINAL MESH EXPOSURE/EROSION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 68903 | PROLIFT PELVIC FLOOR REPAIR | MESH, SURGICAL, POLYMERIC | OTP | ETHICON INC | NA | 3135695 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 46 YR | Required Intervention |