FDA Adverse Event Injury Summary report: N

GYNECARE GYNEMESH* PS

MDR report key: 2772392 · Received October 4, 2012

Report

Report Number
2210968-2012-06046
Event Type
Injury
Date Received
October 4, 2012
Report Date
September 20, 2012
Manufacturer
ETHICON, INC.
Product Code
FTL
PMA / PMN Number
K013718
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). CONCLUSION: 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

(B)(4). IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED VAGINAL PAIN, RECURRING INFECTIONS, DYSPAREUNIA, INCONTINENCE, PAINFUL URINATION, AND BLACKISH BROWN DISCHARGE. IT WAS REPORTED THAT PATIENT CONCURRENTLY UNDERWENT HYSTERECTOMY, SACRAL COLPOPEXY, AND PERINEORRHAPHY.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2010 MESH AND MONARC HAMMOCK WERE USED. THE PATIENT EXPERIENCED PAIN, EROSION OF HER INTERNAL TISSUES, AND SHE HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION IS PROVIDED AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED VAGINAL PAIN, RECURRING INFECTIONS, DYSPAREUNIA, INCONTINENCE, PAINFUL URINATION, AND BLACKISH BROWN DISCHARGE. IT WAS REPORTED THAT PATIENT CONCURRENTLY UNDERWENT HYSTERECTOMY, SACRAL COLPOPEXY, AND PERINEORRHAPHY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GYNECARE GYNEMESH* PS MESH, SURGICAL, POLYMERIC FTL ETHICON, INC. NA BPB640

Patients

Seq Age Sex Outcome Treatment
1 47 YR Required Intervention