FDA Adverse Event Injury Summary report: N

INTERTAN NAIL

MDR report key: 2190052 · Received August 4, 2011

Report

Report Number
1020279-2011-00298
Event Type
Injury
Date Received
August 4, 2011
Date of Event
July 26, 2011
Report Date
August 4, 2011
Manufacturer
SMITH & NEPHEW, INC.
Product Code
JDS
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE NAIL FRACTURED AND A REVISION SURGERY IS BEING PERFORMED TO CORRECT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INTERTAN NAIL NAIL FIXATION JDS SMITH & NEPHEW, INC. 10KM18267

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention