FDA Adverse Event Death Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2190489 · Received July 28, 2011

Report

Report Number
3004209178-2011-82321
Event Type
Death
Date Received
July 28, 2011
Date of Event
July 6, 2011
Report Date
July 6, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

CURRENTLY, IT IS UNK 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 THAT THE CUSTOMER PASSED AWAY. IT WAS STATED THAT SHE WAS WEARING THE INSULIN PUMP BUT IT WAS DISCONNECTED. IT WAS STATED THAT THE CUSTOMER WAS LYING ON TOP OF THE INSULIN PUMP AND IT WAS BEEPING. IT WAS STATED THAT THE CUSTOMER DIED DUE TO NATURAL CAUSES. IT WAS STATED THAT THE LAST RECORD IN CUSTOMER'S BOOK WAS HIGH. NO FURTHER INFO WAS PROVIDED.

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-522CAS

Patients

Seq Age Sex Outcome Treatment
1 Death