FDA Adverse Event Injury Summary report: N

MERSILENE POLYESTER FIBER MESH UNKNOWN PRODUCT

MDR report key: 8928640 · Received August 23, 2019

Report

Report Number
2210968-2019-86086
Event Type
Injury
Date Received
August 23, 2019
Report Date
July 31, 2019
Manufacturer
ETHICON INC.
Product Code
FTL
PMA / PMN Number
PRE-AMEND
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS REPORT IS RELATED TO A JOURNAL ARTICLE; THEREFORE, NO PRODUCT WILL BE RETURNED FOR ANALYSIS AND THE BATCH HISTORY RECORDS CANNOT BE REVIEWED AS THE LOT NUMBER HAS NOT BEEN PROVIDED. THE SINGLE COMPLAINT WAS REPORTED WITH MULTIPLE EVENTS. THERE ARE NO ADDITIONAL DETAILS REGARDING THE ADDITIONAL EVENTS. CITATION: HERNIA (2007) 11:25¿29; DOI: 10.1007/S10029-006-0141-Z; PUBLISHED ONLINE: 11 NOVEMBER 2006. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE WITH TITLE: OUTCOMES OF THE RIVES - STOPPA TECHNIQUE IN INCISIONAL HERNIA REPAIR: TEN YEARS OF EXPERIENCE. THIS RETROSPECTIVE STUDY AIMED TO ASSESS THE OUTCOMES OF IRANIAN PATIENTS UNDERGOING THE R¿S TECHNIQUE AND TO DETERMINE FACTORS AFFECTING RECURRENCE RATE AND TIME. BETWEEN 1993 AND 2003, 86 PATIENTS (MEAN AGE 51.21 YEARS, MALES N=20, FEMALE N=66) WHO HAD UNDERGONE THE CLASSIC R¿S TECHNIQUE FOR VENTRAL INCISIONAL HERNIA WERE INCLUDED IN THIS STUDY. TWO TYPES OF MESH WERE USED, PROLENE AND MERSILENE. COMPLICATIONS INCLUDED SEROMA (N=1) IN WHICH FLUID COLLECTION RESOLVED ON ITS OWN; RECURRENT HERNIA (N=5), SUPERFICIAL WOUND INFECTION (N=10) WHICH WAS TREATED WITH ANTIBIOTICS AND LOCAL CARE; DEEP WOUND INFECTION (N=3) IN WHICH ONE PATIENT NEEDED REMOVAL OF THE MESH AND THE OTHER TWO UNDERWENT ANTIBIOTIC THERAPY, MESH INFECTION (N=2) AND INTESTINAL PARTIAL OBSTRUCTION (N=1). IN CONCLUSION, THE R¿S TECHNIQUE IS THE MOST PROMISING OPEN TECHNIQUE, WITH LOW RECURRENCE RATES, EXCELLENT LONG-TIME RESULTS, AND MINIMAL SERIOUS MORBIDITY. AGE MIGHT BE AN IMPORTANT FACTOR IN RECURRENCE RATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
718773 MERSILENE POLYESTER FIBER MESH UNKNOWN PRODUCT MESH, SURGICAL FTL ETHICON INC.

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention