GYNECARE PROLIFT +M POSTERIOR PELVIC FLOOR REPAIR SYSTEM
Report
- Report Number
- 2210968-2013-10188
- Event Type
- Injury
- Date Received
- June 11, 2013
- Report Date
- June 5, 2013
- Manufacturer
- ETHICON INC.
- Product Code
- OTP
- PMA / PMN Number
- K071512
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
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.
(B)(4).
(B)(4): THE PATIENT UNDERWENT A MESH IMPLANT ON (B)(6) 2010 DUE TO PELVIC ORGAN PROLAPSE, VAGINAL VAULT PROLAPSE, RECTOCELE, STRESS URINARY INCONTINENCE, AND BLADDERNECK HYPERMOBILITY. IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED PAIN, INFECTION, URINARY/BOWEL PROBLEMS, BLEEDING, DYSPAREUNIA AND ABSCESSED COLON. (B)(4).
(B)(4). A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2010 AND MESH AND BOSTON SCIENTIFIC SOLYX MIDURETHRAL SLING WERE IMPLANTED. IT WAS REPORTED THAT SHE 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 |
|---|---|---|---|---|---|---|---|
| 264697 | GYNECARE PROLIFT +M POSTERIOR PELVIC FLOOR REPAIR SYSTEM | MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC | OTP | ETHICON INC. | UNK | 3374758 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention | BOSTON SCIENTIFIC SOLYX MIDURETHRAL SLING| BOSTON SCIENTIFIC SOLYX MIDURETHRAL SLING |