FDA Adverse Event Injury Summary report: N

UKNOWN MESH PRODUCT

MDR report key: 3161882 · Received June 11, 2013

Report

Report Number
2210968-2013-10053
Event Type
Injury
Date Received
June 11, 2013
Report Date
November 11, 2016
Manufacturer
ETHICON INC.
Product Code
OTN
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). 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 CONCURRENTLY WITH I&D OF MULTIPLE INCLUSION CYSTS OF THE VULVA; DUE TO CYSTOCELE, RECTOCELE AND STRESS URINARY INCONTINENCE.

Additional Manufacturer Narrative · 1

(B)(4). ADDITIONAL NARRATIVE: IT WAS REPORTED BY AN ATTORNEY THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2008 AND A MESH WAS IMPLANTED. IT WAS REPORTED THAT PATIENT UNDERWENT REVISION OF PUBOVAGINAL SLING (VAGINAL APPROACH) AND URETHROLYSIS ON (B)(6) 2012 DUE TO VOIDING DYSFUNCTIONS AND PERIURETHRAL FIBROSIS. IT WAS REPORTED THAT PATIENT UNDERWENT URETHRAL MESH EXCISION AND URETHROLYSIS ON (B)(6) 2013 DUE TO PELVIC PAIN, AND HISTORY OF URETHRAL SLING. NO ADDITIONAL INFORMATION WAS PROVIDED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2008 AND MESH WERE IMPLANTED. 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
262306 UKNOWN MESH PRODUCT MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGICAL OTN ETHICON INC. UNK

Patients

Seq Age Sex Outcome Treatment
1 51 YR Required Intervention