UNKNOWN MESH PRODUCT (EWHU)
Report
- Report Number
- 2210968-2013-06320
- Event Type
- Injury
- Date Received
- May 31, 2013
- Report Date
- May 14, 2013
- Manufacturer
- ETHICON, INC.
- Product Code
- FTL
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- ATTORNEY
Narratives
(B)(4). CONCLUSION: NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY.
IT WAS REPORTED THAT PATIENT UNDERWENT MESH EXCISION ON (B)(6) 2004 BY IMPLANTING SURGEON DUE TO ERODED TRANSVAGINAL MESH. IT WAS REPORTED THAT PATIENT UNDERWENT ANOTHER MESH EXCISION ON (B)(6) 2008 BY DR. (B)(6) AND DR. (B)(6) DUE TO RECURRENT CYSTOCELE AND VAGINAL MESH EXTRUSION.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE TO TREAT PELVIC ORGAN PROLAPSE ON (B)(6) 2004 AND MESH WAS IMPLANTED. THE PATIENT EXPERIENCED MULTIPLE COMPLICATIONS, INCLUDING EROSION, FORMATION OF SCAR TISSUE, ADDITIONAL SURGERIES AND NEUROLOGIC COMPROMISE TO HER STRUCTURES AND TISSUES. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
IT WAS REPORTED THAT PATIENT UNDERWENT MESH EXCISION ON (B)(6) 2004 BY IMPLANTING SURGEON DUE TO ERODED TRANSVAGINAL MESH. IT WAS REPORTED THAT PATIENT UNDERWENT ANOTHER MESH EXCISION ON (B)(6) 2008 BY DR. (B)(6) AND DR. (B)(6) DUE TO RECURRENT CYSTOCELE AND VAGINAL MESH EXTRUSION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241400 | UNKNOWN MESH PRODUCT (EWHU) | MESH, SURGICAL, POLYMERIC | FTL | ETHICON, INC. | NA | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 57 YR | Required Intervention |