FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 2945984 · Received February 1, 2013

Report

Report Number
2945984
Event Type
Injury
Date Received
February 1, 2013
Manufacturer
UNK
Product Code
HWC
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

REMOVAL OF TWO SCREWS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
44650 UNK UNK HWC UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 54 YR Hospitalization