FDA Adverse Event Injury Summary report: N

PUMP MMT-722NAP PRDGM INS V2.2 PL EN

MDR report key: 1760438 · Received July 13, 2010

Report

Report Number
3004209178-2010-81976
Event Type
Injury
Date Received
July 13, 2010
Date of Event
June 27, 2010
Report Date
June 27, 2010
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
LZG
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WA, 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

IT WAS REPORTED THAT THE CUSTOMER WAS HOSPITALIZED FOR DIABETES KETOACIDOSIS. THE BLOOD GLUCOSE READING WAS OVER 600MG/DL. TROUBLESHOOTING WAS PERFORMED. THE PROGRAMMING, TIME, BASALS, DAILY TOTALS AND BOLUS HISTORY MATCHED. RAN A FIXED PRIME AND HIGH PRESSURE TESTS AND PASSED. NO FURTHER INFO WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP MMT-722NAP PRDGM INS V2.2 PL EN INFUSION PUMP LZG MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-722NAP

Patients

Seq Age Sex Outcome Treatment
1 20 YR Hospitalization