FDA Adverse Event Injury Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 2072549 · Received April 21, 2011

Report

Report Number
3004209178-2011-81153
Event Type
Injury
Date Received
April 21, 2011
Date of Event
April 5, 2011
Report Date
April 7, 2011
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Adverse Event
Yes
Report Source
Manufacturer report
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. THE DEVICE HAS BEEN RETURNED, BUT NOT YET EVALUATED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER WAS HOSPITALIZED FOR DIABETIC KETOACIDOSIS, WITH A BLOOD GLUCOSE READING OF 385 MG/DL. THE CUSTOMER STATED THAT SHE HAD BEEN HAVING UNEXPLAINED HIGH BLOOD GLUCOSE LEVELS FOR THE PAST MONTH BEFORE THE EVENT. THE CUSTOMER ALSO STATED THAT SHE USES A MODEL MMT-397 QUICK-SET INFUSION SET. PROGRAMMING WAS CORRECT. TROUBLESHOOTING WAS PERFORMED AND THE INSULIN PUMP PASSED THE FIXED PRIME TEST. 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-522NAL

Patients

Seq Age Sex Outcome Treatment
1 20 YR Hospitalization MODEL MMT-397, LOT 9201238| UNOMEDICAL QUICK-SET INSULIN INFUSION SET: