FDA Adverse Event Injury Summary report: N

PROLIFT +M PELVIC FLOOR REPAIR

MDR report key: 2870526 · Received December 12, 2012

Report

Report Number
2210968-2012-07956
Event Type
Injury
Date Received
December 12, 2012
Report Date
November 23, 2012
Manufacturer
ETHICON, INC.
Product Code
OTP
PMA / PMN Number
K071512
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NJ, 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

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND MESH WAS IMPLANTED DUE TO CYSTOCELE. IT WAS REPORTED THAT FOLLOWING INSERTION THE PATIENT EXPERIENCED FOUL ODOR, EROSION AND LEAKAGE. IT WAS ALSO REPORTED THAT THE PATIENT UNDERWENT MESH PROCEDURE ON (B)(6) 2011 FOR EROSION, BLEEDING, ODOR AND PAINFUL INTERCOURSE. (B)(4).

Additional Manufacturer Narrative · 1

IT WAS REPORTED THAT PATIENT UNDERWENT CONCURRENT CYSTOSCOPY PROCEDURE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2009 AND MESH WAS USED. THE PATIENT EXPERIENCED PAIN, EROSION OF HER INTERNAL BODILY TISSUE AND OTHER INJURIES, AND SHE HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES. NO ADDITIONAL INFORMATION IS PROVIDED AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROLIFT +M PELVIC FLOOR REPAIR MESH, SURGICAL, POLYMERIC OTP ETHICON, INC. NA 3342496

Patients

Seq Age Sex Outcome Treatment
1 55 YR Required Intervention