GYNECARE GYNEMESH* PS
Report
- Report Number
- 2210968-2012-06046
- Event Type
- Injury
- Date Received
- October 4, 2012
- Report Date
- September 20, 2012
- Manufacturer
- ETHICON, INC.
- Product Code
- FTL
- PMA / PMN Number
- K013718
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, 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. IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.
(B)(4). IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED VAGINAL PAIN, RECURRING INFECTIONS, DYSPAREUNIA, INCONTINENCE, PAINFUL URINATION, AND BLACKISH BROWN DISCHARGE. IT WAS REPORTED THAT PATIENT CONCURRENTLY UNDERWENT HYSTERECTOMY, SACRAL COLPOPEXY, AND PERINEORRHAPHY.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2010 MESH AND MONARC HAMMOCK WERE USED. THE PATIENT EXPERIENCED PAIN, EROSION OF HER INTERNAL TISSUES, AND SHE HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION IS PROVIDED AT THIS TIME.
IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED VAGINAL PAIN, RECURRING INFECTIONS, DYSPAREUNIA, INCONTINENCE, PAINFUL URINATION, AND BLACKISH BROWN DISCHARGE. IT WAS REPORTED THAT PATIENT CONCURRENTLY UNDERWENT HYSTERECTOMY, SACRAL COLPOPEXY, AND PERINEORRHAPHY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GYNECARE GYNEMESH* PS | MESH, SURGICAL, POLYMERIC | FTL | ETHICON, INC. | NA | BPB640 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 47 YR | Required Intervention |