FDA Adverse Event Injury Summary report: N

PUMP MMT-723NAP PRDGM INSULIN PURPLE EN

MDR report key: 1791788 · Received August 4, 2010

Report

Report Number
3004209178-2010-82361
Event Type
Injury
Date Received
August 4, 2010
Date of Event
July 16, 2010
Report Date
July 16, 2010
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
LZG
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NURSE

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 THAT THE CUSTOMER WAS HOSPITALIZED FOR DIABETES KETOACIDOSIS. THE CUSTOMER WAS TREATED WITH INSULIN DRIP. IT WAS STATED THAT THE CUSTOMER'S BLOOD GLUCOSE WAS HIGH FOR THE PAST FOUR DAYS. NO FURTHER INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP MMT-723NAP PRDGM INSULIN PURPLE EN INFUSION PUMP LZG MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-723NAP

Patients

Seq Age Sex Outcome Treatment
1 53 YR Hospitalization