FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 3230946 · Received July 17, 2013

Report

Report Number
3005477969-2013-00290
Event Type
Injury
Date Received
July 17, 2013
Date of Event
October 23, 2012
Report Date
July 17, 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
331548 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS LTD 54036 040

Patients

Seq Age Sex Outcome Treatment
1 67 YR Hospitalization| R FEMORAL HEAD, # 74121150, LOT # 55493 042