GYNECARE TVT OBURATOR SYSTEM
Report
- Report Number
- 2210968-2013-10068
- Event Type
- Injury
- Date Received
- June 11, 2013
- Report Date
- June 16, 2016
- Manufacturer
- ETHICON INC.
- Product Code
- OTN
- PMA / PMN Number
- K033568
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- OTHER
Narratives
THE PATIENT EXPERIENCED PAIN, EROSION, EXTRUSION, RECURRENCE, DYSPAREUNIA, NEUROMUSCULAR PROBLEMS. IT WAS REPORTED THAT THE PATIENT UNDERWENT MESH REMOVAL ON (B)(6) 2012, DUE TO EXTRUSION. (B)(4).
(B)(4). IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.
IT WAS REPORTED THAT PATIENT UNDERWENT AN AUTOLOGOUS RECTUS FASCIA SLING PROCEDURE, EXTENSIVE DEBRIDEMENT OF EXTRUDED PREVIOUS MIDURETERAL SLING AND A CYSTOSCOPY ON (B)(6) 2012. IT WAS REPORTED THAT PATIENT UNDERWENT AN AUTOLOGOUS RECTUS FASCIA SLING PROCEDURE, SUPRAPUBIC TUBE PLACEMENT AND CYSTOSCOPY ON (B)(6) 2013.
(B)(4): 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 THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2006 AND MESH WAS IMPLANTED. THE PATIENT 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 |
|---|---|---|---|---|---|---|---|
| 263310 | GYNECARE TVT OBURATOR SYSTEM | MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC | OTN | ETHICON INC. | UNK | 2942473 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 53 YR | Required Intervention |