FDA Adverse Event Injury Summary report: N

TENSION FREE VAGINAL TAPE

MDR report key: 2831067 · Received November 14, 2012

Report

Report Number
2210968-2012-07124
Event Type
Injury
Date Received
November 14, 2012
Report Date
October 23, 2012
Manufacturer
ETHICON, INC.
Product Code
FTL
PMA / PMN Number
K033568
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

(B)(4). IT WAS REPORTED THAT DUE TO PELVIC PAIN, PATIENT UNDERWENT OPERATIVE LAPAROSCOPY WITH EXTENSIVE LYSIS OF ADHESIONS ON (B)(6) 2009.

Additional Manufacturer Narrative · 1

(B)(4): 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.

Additional Manufacturer Narrative · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE AND A SLING WAS IMPLANTED. CONCOMITANTLY THE PATIENT UNDERWENT A PANNICULECTOMY, ABDOMINOPLASTY. IT WAS REPORTED THAT DUE TO PELVIC PAIN, DYSPAREUNIA AND URINARY DISTURBANCES, PATIENT UNDERWENT MESH REMOVAL ON (B)(6) 2011. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND AN OBTURATOR SLING WAS IMPLANTED. THE PATIENT EXPERIENCED MULTIPLE COMPLICATIONS INCLUDING EROSION, FORMATION OF SCAR TISSUE, ADDITIONAL SURGERIES AND NEUROLOGIC COMPROMISE TO HER STRUCTURES AND TISSUES. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TENSION FREE VAGINAL TAPE MESH, SURGICAL, POLYMERIC FTL ETHICON, INC. NA 3146787

Patients

Seq Age Sex Outcome Treatment
1 58 YR Required Intervention