PROLIFT +M PELVIC FLOOR REPAIR
Report
- Report Number
- 2210968-2013-01886
- Event Type
- Injury
- Date Received
- February 28, 2013
- Report Date
- February 6, 2013
- Manufacturer
- ETHICON INC
- Product Code
- OTP
- PMA / PMN Number
- K071512
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, 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. THIS IS ONE OF TWO MEDWATCHES BEING SUBMITTED AS TWO DEVICES WERE INVOLVED IN THIS EVENT. SEE ALSO MEDWATCH 2210968-2013-01885. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.
(B)(4). ADDITIONAL NARRATIVE: THE PATIENT UNDERWENT MESH IMPLANTATION IN ORDER TO TREAT RECTOCELE, ENTEROCELE, VAGINAL VAULT PROLAPSE, WEAKENED RV FASCIA, PELVIC ORGAN PROLAPSE AND STRESS URINARY INCONTINENCE. IT WAS REPORTED THAT THE PATIENT UNDERWENT A MESH TRIMMING IN (B)(6) 2010. IT WAS ALSO REPORTED THAT THE PATIENT UNDERWENT MESH REVISION IN (B)(6) 2010 DUE TO EXPOSED MESH. NO ADDITIONAL INFORMATION WAS PROVIDED. (B)(4) - MESH EXPOSURE.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND A MESH WAS IMPLANTED. THE PATIENT EXPERIENCED PAIN, EROSION OF HER INTERNAL BODILY TISSUE AND OTHER INJURIES FOLLOWING THE PROCEDURE. 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 |
|---|---|---|---|---|---|---|---|
| 87060 | PROLIFT +M PELVIC FLOOR REPAIR | MESH, SURGICAL, POLYMERIC | OTP | ETHICON INC | NA | 3348266 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 56 YR | Required Intervention |