FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

MDR report key: 2040046 · Received March 25, 2011

Report

Report Number
3004209178-2011-80810
Event Type
Malfunction
Date Received
March 25, 2011
Date of Event
March 14, 2011
Report Date
March 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
KS, 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 BY THE CUSTOMER THAT THE INSULIN PUMP WAS GIVING NO DELIVERY ALARMS. THE CUSTOMER STATED THAT SHE HAS CHANGED HER SET SEVERAL TIMES AND WAS STILL RECEIVING NO DELIVERY ALARMS. THE CUSTOMER ALSO STATED THAT WHEN SHE MANUALLY PRIMES, THE PISTON ONLY GOES UP SLIGHTLY. TROUBLESHOOTING WAS PERFORMED AND THE PISTON ANOMALY WAS CONFIRMED. THE INSULIN PUMP FAILED THE DISPLACEMENT TEST AND ALARMED MAX FILL INSTEAD OF NO RESERVOIR. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP MDS MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-723NAH

Patients

Seq Age Sex Outcome Treatment
1 30 YR