FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME INSULIN INFUSION PUMP

MDR report key: 4142042 · Received October 4, 2014

Report

Report Number
2032227-2014-33642
Event Type
Malfunction
Date Received
October 4, 2014
Date of Event
September 4, 2014
Report Date
February 12, 2019
Manufacturer
MEDTRONIC MINIMED
Product Code
OYC
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INSULIN PUMP INVOLVED IN THIS EVENT IS THE PARADIGM REAL-TIME VEO INSULIN INFUSION PUMP, WHICH IS NOT MARKETED IN THE UNITED STATES. HOWEVER, THE DEVICE IS SIMILAR TO THE PARADIGM REAL-TIME INSULIN INFUSION PUMP, WHICH IS MARKETED IN THE UNITED STATES. CURRENTLY, IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. THE DEVICE WILL BE RETURNED FOR ANALYSIS AND FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

Additional Manufacturer Narrative · 1

DEVICE PASSED THE DISPLACEMENT TEST, REWIND TEST, BASIC OCCLUSION TEST, OCCLUSION TEST AND PRIME TEST. HOWEVER, UNEXPECTED NO DELIVERY ALARM DURING EXCESSIVE NO DELIVERY TEST DUE TO FAULTY FORCE SENSOR RESISTOR (GOLD). NO MOTOR ERROR ALARM NOTED. MOTOR PASSED MOTOR TEST.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER HAD A MOTOR ERROR ON THE INSULIN PUMP. CUSTOMER CHANGED THE TUBE AND RESERVOIR. INSULIN WAS NOT CLOUDY OR EXPIRED. ALARM STILL PERSISTS AND CUSTOMER WAS ASKED TO RETURN THE PUMP FOR ANALYSIS. NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
621700 PARADIGM REAL-TIME INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-754LWWS

Patients

Seq Age Sex Outcome Treatment
1