PROLIFT PELVIC FLOOR REPAIR
Report
- Report Number
- 2210968-2013-05941
- Event Type
- Injury
- Date Received
- May 29, 2013
- Report Date
- May 6, 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)
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND MESH WAS IMPLANTED DUE TO LARGE SYMPTOMATIC RECTOCELE.
IT WAS REPORTED THAT THE PATIENT UNDERWENT REMOVAL OF POSTERIOR VAGINAL WALL MESH, COMBINED ANTERIOR AND POSTERIOR REPAIR ON (B)(6) 2014 BY DR. (B)(6) DUE TO CYSTOCELE, RECTOCELE, AND PELVIC PAIN.
(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 THE PATIENT UNDERWENT REMOVAL OF POSTERIOR VAGINAL WALL MESH, COMBINED ANTERIOR AND POSTERIOR REPAIR ON (B)(6) 2014 BY DR. (B)(6) DUE TO CYSTOCELE, RECTOCELE, AND PELVIC PAIN.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 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 |
|---|---|---|---|---|---|---|---|
| 233970 | PROLIFT PELVIC FLOOR REPAIR | MESH, SURGICAL, POLYMERIC | OTP | ETHICON, INC. | NA | 3008714 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Required Intervention |