FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2021989 · Received March 8, 2011

Report

Report Number
3004209178-2011-80603
Event Type
Malfunction
Date Received
March 8, 2011
Date of Event
February 25, 2011
Report Date
February 25, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

CURRENTLY, IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE, THEREFORE, CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.

Description of Event or Problem · 1

IT WAS REPORTED BY THE CUSTOMER THAT HER INSULIN PUMP HAD A FROZEN DISPLAY AND THE BUTTONS WERE NOT RESPONDING. THE CUSTOMER STATED THAT PRIOR TO THE EVENT, THE CUSTOMER HAD REC'D A LOW RESERVOIR ALARM AND FOUND THE BUTTONS DID NOT RESPOND WHEN ATTEMPTING TO CLEAR THE ALARM. THE CUSTOMER ALSO STATED THAT SHE HAD REMOVED THE BATTERY FOR AN HOUR AND INSERTED A NEW BATTERY BUT STILL DID NOT HAVE ANY RESPONSE FROM THE BUTTONS. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP MDS MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-722NAS

Patients

Seq Age Sex Outcome Treatment
1 19 YR