FDA Adverse Event Injury Summary report: N

NA

MDR report key: 2940904 · Received July 13, 2006

Report

Report Number
2940904
Event Type
Injury
Date Received
July 13, 2006
Date of Event
June 28, 2006
Report Date
June 29, 2006
Product Code
FTR
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

SEVEN MONTHS AFTER HAVING BREAST IMPLANTS, THE PATIENT DEVELOPED CELLULITIS OF THE LEFT BREAST.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 NA BREAST IMPLANT FTR

Patients

Seq Age Sex Outcome Treatment
1 51 YR Required Intervention