FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

MDR report key: 4854614 · Received June 18, 2015

Report

Report Number
3004209178-2015-66627
Event Type
Malfunction
Date Received
June 18, 2015
Date of Event
May 16, 2015
Report Date
May 31, 2015
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO.
Product Code
OYC
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX
Reporter Occupation
PATIENT

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

IT WAS REPORTED VIA PHONE CALL, THAT THE CUSTOMER RECEIVED EXCESSIVE NO DELIVERY ALARMS. THE CUSTOMER ALSO MENTIONED THAT THEY HAD A BENT CANNULA. CUSTOMER'S BLOOD GLUCOSE LEVEL AT THE TIME 299 MG/DL. TROUBLESHOOTING OCCURRED. NO SIGNIFICANT EVENT LEADING UP TO THE INCIDENT WAS MENTIONED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
396783 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-723NAL

Patients

Seq Age Sex Outcome Treatment
1 65 YR