FDA Adverse Event Injury Summary report: N

R/T LOCK NAIL-FEM SE

MDR report key: 1973630 · Received January 31, 2011

Report

Report Number
1020279-2011-00019
Event Type
Injury
Date Received
January 31, 2011
Report Date
January 31, 2011
Manufacturer
SMITH & NEPHEW, INC.
Product Code
LXH
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE DEVICE COULD NOT BE INSTALLED AND DELAYED SURGERY 30-60 MINUTES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 R/T LOCK NAIL-FEM SE NAIL CAP LXH SMITH & NEPHEW, INC. 07JM05130

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization