FDA Adverse Event Injury Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2033804 · Received March 17, 2011

Report

Report Number
3004209178-2011-80709
Event Type
Injury
Date Received
March 17, 2011
Date of Event
March 5, 2011
Report Date
March 5, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED REL
Product Code
MDS
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. 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 WAS HOSPITALIZED FOR HYPOGLYCEMIA, WITH A BLOOD GLUCOSE READING OF 130 MG/DL. THE CUSTOMER'S WIFE STATED THAT THE CUSTOMER OFTEN EXPERIENCED LOW BLOOD GLUCOSE LEVELS IN THE MORNING. THE CUSTOMER'S WIFE ALSO STATED THAT THE LAST SET CHANGE WAS 3 DAYS PRIOR TO THE EVENT. PROGRAMMING WAS CORRECT. 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 59 YR Hospitalization