FDA Adverse Event Malfunction Summary report: N

*

MDR report key: 796645 · Received December 11, 2006

Report

Report Number
796645
Event Type
Malfunction
Date Received
December 11, 2006
Date of Event
November 29, 2006
Report Date
December 1, 2006
Manufacturer
SRI/SURGICAL EXPRESS, INC.
Product Code
LRW
Product Problem
Yes
Report Source
User Facility report
Reporter Location
NC, US

Narratives

Description of Event or Problem · 1

DURING PLANTAR FASCITIS PROCEDURE, TIP OF IRIS SCISSORS BROKE OFF. TIP RETRIEVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * INSTRUMENT, SCISSORS LRW SRI/SURGICAL EXPRESS, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 33 YR