FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 3231224 · Received July 17, 2013

Report

Report Number
2032227-2013-02963
Event Type
Malfunction
Date Received
July 17, 2013
Date of Event
June 25, 2013
Report Date
June 25, 2013
Manufacturer
MEDTRONIC MINIMED
Product Code
OYC
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INSULIN PUMP ALARMED DURING THE BASIC OCCLUSION TEST DUE TO A PROTRUDED/LOOSE DRIVE SUPPORT DISK.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INSULIN PUMP GAVE AN ALARM MULTIPLE TIMES DURING THE MANUAL PRIME PROCESS. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
330560 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-722CAL

Patients

Seq Age Sex Outcome Treatment
1