FDA Adverse Event Injury Summary report: N

TENSION FREE VAGINAL TAPE

MDR report key: 2760487 · Received September 26, 2012

Report

Report Number
2210968-2012-05638
Event Type
Injury
Date Received
September 26, 2012
Report Date
September 7, 2012
Manufacturer
ETHICON, INC.
Product Code
FTL
PMA / PMN Number
K052401
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
ATTORNEY

Narratives

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

(B)(4). IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE AND MESH WAS IMPLANTED ON (B)(6) 2007 IN ORDER TO TREAT CYSTOCELE, STRESS URINARY INCONTINENCE, RECTOCELE, VAGINAL ATROPHY, VAGINAL LESION, PAIN, AND DYSPAREUNIA. NO ADDITIONAL INFORMATION WAS PROVIDED.

Additional Manufacturer Narrative · 1

(B)(4): IT WAS REPORTED THAT DUE TO VAGINAL/STOMACH PAIN, DYSPAREUNIA AND VAGINAL DISCHARGE THE PATIENT UNDERWENT PARTIAL MESH REMOVAL ON (B)(6) 2012.(B)(4).

Additional Manufacturer Narrative · 1

IT WAS REPORTED THAT PATIENT UNDERWENT CONCURRENT CYSTOURETHROSCOPY PROCEDURE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2007 AND MESH AND BARD MESH WERE USED. 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
1 TENSION FREE VAGINAL TAPE MESH, SURGICAL, POLYMERIC FTL ETHICON, INC. NA NI

Patients

Seq Age Sex Outcome Treatment
1 62 YR Required Intervention