FDA Adverse Event Injury Summary report: N

PROLIFT PELVIC FLOOR REPAIR

MDR report key: 2963606 · Received February 15, 2013

Report

Report Number
2210968-2013-01197
Event Type
Injury
Date Received
February 15, 2013
Report Date
January 23, 2013
Manufacturer
ETHICON INC
Product Code
OTP
PMA / PMN Number
K013718
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

(B)(4): 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 CRITERIATHIS IS ONE OF TWO MEDWATCHES BEING SUBMITTED AS TWO DEVICES WERE INVOLVED IN THIS EVENT. SEE ALSO MEDWATCH 2210968-2013-01195. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.

Additional Manufacturer Narrative · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT VAGINAL MESH REMOVAL/REVISION AND A CYSTOSCOPY ON (B)(6) 2012 BY DR. (B)(6), DUE TO VAGINAL MESH EXPOSURE/EROSION.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND A MESH WAS IMPLANTED. THE PATIENT EXPERIENCED PAIN, MESH EROSION, INFECTION, BLEEDING, VAGINAL SCARRING/SHRINKAGE AND EXPOSURE/EXTRUSION/PROTRUSION, THE PATIENT 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 THE PATIENT UNDERWENT VAGINAL MESH REMOVAL/REVISION AND A CYSTOSCOPY ON (B)(6) 2012 BY DR. (B)(6), DUE TO VAGINAL MESH EXPOSURE/EROSION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
68903 PROLIFT PELVIC FLOOR REPAIR MESH, SURGICAL, POLYMERIC OTP ETHICON INC NA 3135695

Patients

Seq Age Sex Outcome Treatment
1 46 YR Required Intervention