FDA Adverse Event Malfunction Summary report: N

PUMP MMT-722NAS PRDGM INS V2.2 SK EN

MDR report key: 1810983 · Received August 9, 2010

Report

Report Number
3004209178-2010-82404
Event Type
Malfunction
Date Received
August 9, 2010
Date of Event
July 9, 2010
Report Date
July 27, 2010
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS MED-REL
Product Code
MDS
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

FAILURE ANALYSIS REVEALED THAT THE INSULIN PUMP HAD A BLANK DISPLAY AS A RESULT OF MOISTURE DAMAGE FOUND ON THE ELECTRONIC AND MOTOR ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INSULIN PUMP HAD A BLACK SCREEN. TROUBLESHOOTING WAS PERFORMED. IT WAS STATED THAT THE DEVICE WAS EXPOSED TO HOT TEMPERATURES. THE MOTHER ALSO REPORTED THAT THE CUSTOMER WAS IN THE POOL WHILE WEARING THE INSULIN PUMP. NO FURTHER INFORMATION WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP MMT-722NAS PRDGM INS V2.2 SK EN INFUSION PUMP MDS MEDTRONIC PUERTO RICO OPERATIONS MED-REL MMT-722NAS

Patients

Seq Age Sex Outcome Treatment
1 16 YR