FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2082052 · Received April 26, 2011

Report

Report Number
3004209178-2011-81217
Event Type
Malfunction
Date Received
April 26, 2011
Date of Event
April 14, 2011
Report Date
April 14, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
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. THE DEVICE WILL BE RETURNED FOR ANALYSIS AND FURTHER INFO WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER HAD AN INSULIN PUMP THAT DID NOT DELIVER INSULIN CORRECTLY. THE CUSTOMER STATED THAT HE TREATED HIS HIGH BLOOD GLUCOSE LEVELS WITH THE INSULIN PUMP AND IT DID NOT LOWER HIS BLOOD GLUCOSE. LEVELS. 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 45 YR