FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 3231552 · Received July 17, 2013

Report

Report Number
3005477969-2013-00296
Event Type
Injury
Date Received
July 17, 2013
Date of Event
September 7, 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. IMPAIRED FUNCTION AND REDUCED WALKING TIME REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
331569 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS LTD 64829 036

Patients

Seq Age Sex Outcome Treatment
1 57 YR Hospitalization| R FEMORAL HEAD, # 74121146, LOT # 67028 019