FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 2946053 · Received February 1, 2013

Report

Report Number
2946053
Event Type
Injury
Date Received
February 1, 2013
Date of Event
March 6, 2012
Report Date
November 10, 2012
Manufacturer
UNK
Product Code
FTR
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REMOVAL OF BILATERAL SALINE BREAST IMPLANTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
45102 UNK UNK FTR UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 55 YR Hospitalization