FDA Adverse Event Injury Summary report: N

SURGIMESH XB BG MEDICAL

MDR report key: 16489024 · Received March 3, 2023

Report

Report Number
MW5115459
Event Type
Injury
Date Received
March 3, 2023
Date of Event
February 21, 2023
Report Date
March 1, 2023
Manufacturer
MEDICAL MURRAY, INC.
Product Code
FTL
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

SURGIMESH PLACED ON (B)(6) 2021, INFECTION IDENTIFIED (B)(6) 2021. 1 YEAR TREATMENT WITH INFECTIOUS DISEASE, SURGEON, ANTIBIOTIC THERAPY. MESHED WAS REMOVED (B)(6) 2023. CT(COMPUTED TOMOGRAPHY) ABDOMEN: LARGE ABDOMINAL WALL FLUID COLLECTION UNDERLYING THE SURGICAL MESH. MEASURING 5.9 X 10.2 APPROXIMATELY. DRAIN PLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
626850 SURGIMESH XB BG MEDICAL MESH, SURGICAL, POLYMERIC FTL MEDICAL MURRAY, INC. Z2459D18C

Patients

Seq Age Sex Outcome Treatment
1 70 YR Male Required Intervention| H