FDA Adverse Event Injury Summary report: N

GYNECARE TVT-AA ABDOMINAL

MDR report key: 3233552 · Received July 18, 2013

Report

Report Number
2210968-2013-13638
Event Type
Injury
Date Received
July 18, 2013
Report Date
March 22, 2016
Manufacturer
ETHICON INC.
Product Code
OTN
PMA / PMN Number
K012628
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

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).

Additional Manufacturer Narrative · 1

ADDITIONAL NARRATIVE: IT WAS REPORTED THAT PATIENT UNDERWENT REMOVAL OF THE SLING, HYSTEROSCOPY AND D&C ON (B)(6) 2015 DUE TO PELVIC PAIN AND MENOMETRORRHAGIA.

Additional Manufacturer Narrative · 1

IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2004 AND A MESH WAS IMPLANTED DUE TO SUI. IT WAS REPORTED THAT DURING THE PROCEDURE THE BLADDER WAS PUNCTURED WITH INSERTION OF TROCAR IN LEFT SIDE. IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED RECURRENCE, URINARY PROBLEMS AND VAGINAL SCARRING. NO ADDITIONAL INFORMATION WAS PROVIDED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2004 AND MESH WAS 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
335616 GYNECARE TVT-AA ABDOMINAL MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC OTN ETHICON INC. UNK 1125524

Patients

Seq Age Sex Outcome Treatment
1 36 YR Required Intervention