FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 5211972 · Received November 9, 2015

Report

Report Number
2032227-2015-64324
Event Type
Malfunction
Date Received
November 9, 2015
Date of Event
October 27, 2015
Report Date
October 27, 2015
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO.
Product Code
OYC
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

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. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT CUSTOMER RECEIVED AN UNEXPECTED RESTART ALARM WITH EACH BATTERY CHANGE AND TIME AND DATE WOULD NEED TO BE REPROGRAMMED. CUSTOMER WAS ADVISED TO CLEAN BATTERY COMPARTMENT AND THAT BATTERY CAP WOULD BE REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
742999 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-722CAS

Patients

Seq Age Sex Outcome Treatment
1