FDA Adverse Event Injury Summary report: N

UNKNOWN MESH PRODUCT (EWHU)

MDR report key: 3140073 · Received May 31, 2013

Report

Report Number
2210968-2013-06320
Event Type
Injury
Date Received
May 31, 2013
Report Date
May 14, 2013
Manufacturer
ETHICON, INC.
Product Code
FTL
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, 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

IT WAS REPORTED THAT PATIENT UNDERWENT MESH EXCISION ON (B)(6) 2004 BY IMPLANTING SURGEON DUE TO ERODED TRANSVAGINAL MESH. IT WAS REPORTED THAT PATIENT UNDERWENT ANOTHER MESH EXCISION ON (B)(6) 2008 BY DR. (B)(6) AND DR. (B)(6) DUE TO RECURRENT CYSTOCELE AND VAGINAL MESH EXTRUSION.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE TO TREAT PELVIC ORGAN PROLAPSE ON (B)(6) 2004 AND MESH 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.

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENT UNDERWENT MESH EXCISION ON (B)(6) 2004 BY IMPLANTING SURGEON DUE TO ERODED TRANSVAGINAL MESH. IT WAS REPORTED THAT PATIENT UNDERWENT ANOTHER MESH EXCISION ON (B)(6) 2008 BY DR. (B)(6) AND DR. (B)(6) DUE TO RECURRENT CYSTOCELE AND VAGINAL MESH EXTRUSION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241400 UNKNOWN MESH PRODUCT (EWHU) MESH, SURGICAL, POLYMERIC FTL ETHICON, INC. NA NI

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention