FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 3021295 · Received March 26, 2013

Report

Report Number
3005477969-2013-00116
Event Type
Injury
Date Received
March 26, 2013
Date of Event
October 16, 2010
Report Date
March 26, 2013
Manufacturer
SMITH & NEPHEW ORTHOPAEDICS LTD
Product Code
NXT
PMA / PMN Number
P040033
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
124053 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS LTD 73143 020

Patients

Seq Age Sex Outcome Treatment
1 34 YR Hospitalization| R FEMORAL HEAD, # 74121146, LOT # 69005 039