FDA Adverse Event Malfunction Summary report: N

PUMP MMT-722LNAH PRDGM INS BL EN ML

MDR report key: 1850169 · Received September 22, 2010

Report

Report Number
2032227-2010-82715
Event Type
Malfunction
Date Received
September 22, 2010
Date of Event
September 1, 2010
Report Date
September 1, 2010
Manufacturer
MEDTRONIC MINIMED
Product Code
MDS
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE INSULIN PUMP WAS RECEIVED WITH A FROZEN DISPLAY DUE TO CORROSION ON THE MOTHER BOARD.

Description of Event or Problem · 1

THE CUSTOMER REPORTED UNRESPONSIVE BUTTONS AND A FROZEN SCREEN. TROUBLESHOOTING WAS PERFORMED, BUT THE ISSUES WERE NOT RESOLVED. ADVISED THAT THE INSULIN PUMP WOULD BE REPLACED. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP MMT-722LNAH PRDGM INS BL EN ML INFUSION PUMP MDS MEDTRONIC MINIMED MMT-722LNAH

Patients

Seq Age Sex Outcome Treatment
1 15 YR