FDA Adverse Event Injury Summary report: N

0123680-COMPOSIX MESH E/X

MDR report key: 427874 · Received November 9, 2002

Report

Report Number
1213643-2002-00054
Event Type
Injury
Date Received
November 9, 2002
Report Date
November 8, 2002
Manufacturer
C.R. BARD, INC. (PUERTO RICO)
Product Code
FTL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PT INFECTION - IDENTIFIED AS MRSA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 0123680-COMPOSIX MESH E/X 350101104-MESH COMPOSIX FTL C.R. BARD, INC. (PUERTO RICO) * 41DLDP15

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention