FDA Adverse Event Injury Summary report: N

BHR

MDR report key: 2091538 · Received May 17, 2011

Report

Report Number
3005477969-2011-00104
Event Type
Injury
Date Received
May 17, 2011
Report Date
May 17, 2011
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 IDENTIFIED THAT A REVISION SURGERY WAS PERFORMED IN (B)(6) 2010.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BHR ACETABULAR CUP NXT SMITH & NEPHEW ORTHOPAEDICS, LTD.

Patients

Seq Age Sex Outcome Treatment
1 54 YR Hospitalization| R FEMORAL HEAD, PART AND LOT UNKNOWN