FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2863212 · Received December 10, 2012

Report

Report Number
3004209178-2012-91166
Event Type
Malfunction
Date Received
December 10, 2012
Date of Event
October 1, 2012
Report Date
November 26, 2012
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO.
Product Code
CGA
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

FAILURE ANALYSIS REVEALED THAT THE INSULIN PUMP ALARMED DURING THE BASIC OCCLUSION TEST AS A RESULT OF A LOOSE DRIVE SUPPORT DISK. THE DEVICE HAD ALSO INTERMITTENT RESPONSE DURING TESTING DUE TO A CORRODED KEYPAD TRACE.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER'S INSULIN PUMP ALARMED, AND HAVING ISSUES DURING PRIME/REWIND. ADVISED THE CALLER THAT THE INSULIN PUMP WOULD BE REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PARADIGM REAL-TIME INSULIN INFUSION PUMP OYC CGA MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-722WWS

Patients

Seq Age Sex Outcome Treatment
1