FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 2946023 · Received February 1, 2013

Report

Report Number
2946023
Event Type
Injury
Date Received
February 1, 2013
Date of Event
September 19, 2012
Report Date
January 29, 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

TWO SCREWS FROM LEFT FOOT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
43771 UNK UNK HWC UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 67 YR Hospitalization