TENSION FREE VAGINAL TAPE
Report
- Report Number
- 2210968-2013-03553
- Event Type
- Injury
- Date Received
- April 8, 2013
- Report Date
- March 19, 2013
- Manufacturer
- ETHICON, INC.
- Product Code
- PAH
- PMA / PMN Number
- K052401
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, 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 CRITERIA. THIS IS ONE OF TWO MEDWATCHES BEING SUBMITTED AS TWO DEVICES WERE INVOLVED IN THIS EVENT. SEE ALSO MEDWATCH 2210968-2013-03554. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.
(B)(4). IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED EXTRUSION, INFECTION, URINARY/BOWEL PROBLEMS, RECURRENCE, BLEEDING, AND VAGINAL SCARRING. IT WAS REPORTED THAT THE PATIENT UNDERWENT AN EXCISION OF MESH ON (B)(6) 2007 CONCURRENTLY WITH POSTERIOR COLPORRHAPHY; DUE TO MESH EXPOSURE, URINARY OBSTRUCTION, INCONTINENCE, PAIN AND DISCOMFORT. (B)(4).
IT WAS REPORTED THAT THE PATIENT UNDERWENT A SURGICAL PROCEDURE ON (B)(6) 2007 AND MESH WAS IMPLANTED. IT WAS REPORTED THAT SHE EXPERIENCED PAIN, EROSION OF HER INTERNAL BODILY TISSUE AND OTHER INJURIES FOLLOWING THE PROCEDURE. IT WAS REPORTED THAT THE PATIENT HAS UNDERGONE MULTIPLE SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 144153 | TENSION FREE VAGINAL TAPE | MESH, SURGICAL, POLYMERIC | PAH | ETHICON, INC. | NA | 2981420 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Required Intervention |