FDA Adverse Event Injury Summary report: N

GYNECARE TVT OBTURATOR SYSTEM

MDR report key: 3242400 · Received July 23, 2013

Report

Report Number
2210968-2013-14093
Event Type
Injury
Date Received
July 23, 2013
Report Date
November 16, 2017
Manufacturer
ETHICON INC.
Product Code
OTN
PMA / PMN Number
K033568
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE AND MESH WAS IMPLANTED ALONG WITH CONCURRENT LAVH AND RSO DUE TO SUI, UTERINE FIBROIDS, MENORRHAGIA AND SEVERE DYSMENORRHEA. IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED PAIN, EROSION, , INFECTION, URINARY/BOWEL PROBLEMS, FISTULAE, DYSPAREUNIA, NEUROMUSCULAR PROBLEMS , VAGINAL SCARRING VAGINAL SHRINKAGE AND EMOTIONAL PROBLEMS. IT WAS REPORTED THAT PATIENT UNDERWENT MESH REVISION ON (B)(6) 2007 DUE TO EROSION. (B)(4). A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.

Additional Manufacturer Narrative · 1

(B)(4). CONCLUSION: NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY.

Additional Manufacturer Narrative · 1

.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2007 AND MESH WAS IMPLANTED INTO THE PATIENT. IT IS ALSO REPORTED THAT THE PATIENT EXPERIENCED PAIN, EROSION OF INTERNAL TISSUES, AND HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION IS PROVIDED AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
342908 GYNECARE TVT OBTURATOR SYSTEM MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC OTN ETHICON INC. UNK 3011384

Patients

Seq Age Sex Outcome Treatment
1 44 YR Required Intervention