FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 2893953 · Received January 3, 2013

Report

Report Number
3005477969-2013-00006
Event Type
Injury
Date Received
January 3, 2013
Date of Event
December 20, 2012
Report Date
January 3, 2013
Manufacturer
SMITH & NEPHEW ORTHOPAEDICS LTD
Product Code
NXT
PMA / PMN Number
P040033
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO A FEMORAL NECK FRACTURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2726 BHR FEMORAL HEAD NXT SMITH & NEPHEW ORTHOPAEDICS LTD 08JW19082

Patients

Seq Age Sex Outcome Treatment
1 60 YR Hospitalization| R