FDA Adverse Event Injury Summary report: N

BARD

MDR report key: 2597586 · Received May 29, 2012

Report

Report Number
MW5025618
Event Type
Injury
Date Received
May 29, 2012
Date of Event
February 4, 2010
Report Date
May 29, 2012
Manufacturer
N.J RAM MEDICAL INC.
Product Code
FTL
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

MESH HERNIA PATCH. DIAGNOSIS FOR USE: ING HERNIA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BARD MESH PATCH FTL N.J RAM MEDICAL INC. NOT SURE

Patients

Seq Age Sex Outcome Treatment
1 41 YR Other| R