FDA Adverse Event Injury Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2041932 · Received March 29, 2011

Report

Report Number
2032227-2011-00784
Event Type
Injury
Date Received
March 29, 2011
Date of Event
January 25, 2011
Report Date
March 15, 2011
Manufacturer
MEDTRONIC MINIMED
Product Code
MDS
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OK, 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 STATED THAT HE WAS HOSPITALIZED WITH A BLOOD GLUCOSE READING OF 22 MG/DL. PRIOR TO BEING HOSPITALIZED, THE CUSTOMER FELL OFF THE COUCH AND BROKE HIS HIP AFTER HE EXPERIENCED HYPOGLYCEMIA. NO TROUBLESHOOTING WAS PERFORMED AS THE INSULIN PUMP BEING WORN AT THE TIME OF THE EVENT, HAD ALREADY BEEN REPLACED. 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 MINIMED MMT-522LNAS

Patients

Seq Age Sex Outcome Treatment
1 49 YR Hospitalization