FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 3251674 · Received July 29, 2013

Report

Report Number
3005477969-2013-00321
Event Type
Injury
Date Received
July 29, 2013
Date of Event
August 29, 2012
Report Date
July 29, 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 DUE IMPAIRED FUNCTION AND RANGE OF MOTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352184 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS LTD 83859 007

Patients

Seq Age Sex Outcome Treatment
1 53 YR FEMORAL HEAD, # 74121146, LOT # 79080 031