FDA Adverse Event Injury Summary report: N

INTERTAN NAILS

MDR report key: 2970287 · Received February 20, 2013

Report

Report Number
1020279-2013-00110
Event Type
Injury
Date Received
February 20, 2013
Date of Event
February 15, 2013
Report Date
February 15, 2013
Manufacturer
SMITH & NEPHEW, INC.
Product Code
JDS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED WHILE ENGAGING\DISENGAGING THE DEVICE INTRA-OPERATIVELY, THERE WAS A DELAY OF SURGERY TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
73133 INTERTAN NAILS 10MM X 18CM 125D JDS SMITH & NEPHEW, INC. 12LM02552

Patients

Seq Age Sex Outcome Treatment
1 80 YR Hospitalization| R