FDA Adverse Event Malfunction Summary report: N

GUARDIAN REAL-TIME MONITIOR

MDR report key: 4140786 · Received October 3, 2014

Report

Report Number
2032227-2014-32690
Event Type
Malfunction
Date Received
October 3, 2014
Date of Event
September 3, 2014
Report Date
September 3, 2014
Manufacturer
MEDTRONIC MINIMED
Product Code
MDS
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
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.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE DISPLAY OF THE GUARDIAN WAS MILKY. NO FURTHER INFORMATION REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
620121 GUARDIAN REAL-TIME MONITIOR CGM MDS MEDTRONIC MINIMED CSS7100WW

Patients

Seq Age Sex Outcome Treatment
1