FDA Adverse Event Injury Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2202425 · Received August 4, 2011

Report

Report Number
3004209178-2011-82406
Event Type
Injury
Date Received
August 4, 2011
Date of Event
July 20, 2011
Report Date
July 21, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MD, 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. WE THEREFORE, CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED BEING HOSPITALIZED DUE TO HYPOGLYCEMIA. THE BLOOD GLUCOSE READING WAS 19MG/DL. THE CUSTOMER STATED THAT HE PASSED OUT. THE CUSTOMER STATED THAT SHE WOKE UP IN THE MORNING WITH LOW GLUCOSE OF 70MG/DL, AND HAD BREAKFAST, BUT SHE DID NOT BOLUS FOR BREAKFAST. NO FURTHER INFORMATION 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-522NAP

Patients

Seq Age Sex Outcome Treatment
1 44 YR Hospitalization