FDA Adverse Event Injury Summary report: N

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

MDR report key: 2202300 · Received August 2, 2011

Report

Report Number
3004209178-2011-82393
Event Type
Injury
Date Received
August 2, 2011
Date of Event
July 16, 2011
Report Date
July 20, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
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

THE CUSTOMER REPORTED BEING AT THE CLINIC FOR HIGH BLOOD GLUCOSE OF 363MG/DL. THE CUSTOMER STATED THAT HE DISCUSSED WITH HIS HEALTH CARE PROFESSIONAL TRAINING FOUR DAYS BEFORE THE EVENT, AND HE WAS ADVISED TO ADJUST HIS BASAL RATES. THE CUSTOMER STATED THAT HE WAS EXPERIENCING UNEXPLAINED HIGH GLUCOSE FOR THE PAST FIVE DAYS. THE CUSTOMER'S MOST RECENT GLUCOSE READING WAS 390MG/DL, AND WAS TREATED WITH THE INSULIN PUMP AND MANUAL INJECTIONS. TROUBLESHOOTING WAS PERFORMED. THE PROGRAMMING, TIME, AND DATE WERE CORRECT. RAN A FIXED PRIME AND HIGH PRESSURE TEST AND THE INSULIN PUMP PASSED THE TESTS. NO FURTHER INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP MDS MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-723NAS

Patients

Seq Age Sex Outcome Treatment
1 66 YR Hospitalization