FDA Adverse Event Malfunction Summary report: N

CADD-LEGACY

MDR report key: 3001624 · Received January 21, 2013

Report

Report Number
3001624
Event Type
Malfunction
Date Received
January 21, 2013
Date of Event
December 26, 2012
Report Date
January 21, 2013
Manufacturer
SMITHS MEDICAL ASD, INC.
Product Code
FRN
Product Problem
Yes
Report Source
User Facility report
Reporter Location
RI, US

Narratives

Description of Event or Problem · 1

PUMP WAS FOUND TO BE ON STOPPED MODE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
28916 CADD-LEGACY PUMP, INFUSION FRN SMITHS MEDICAL ASD, INC. 6400 *

Patients

Seq Age Sex Outcome Treatment
1 *