FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 2946034 · Received February 1, 2013

Report

Report Number
2946034
Event Type
Injury
Date Received
February 1, 2013
Date of Event
October 16, 2012
Report Date
February 1, 2013
Manufacturer
UNK
Product Code
UNK
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REMOVAL OF FIVE SCREWS AND ONE PLATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
45300 UNK UNK UNK UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 45 YR Hospitalization