FDA Adverse Event Malfunction Summary report: N

PARADIGM INSULIN INFUSION PUMP

MDR report key: 2791889 · Received October 15, 2012

Report

Report Number
3004209178-2012-90105
Event Type
Malfunction
Date Received
October 15, 2012
Date of Event
August 21, 2012
Report Date
October 5, 2012
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO.
Product Code
LZG
PMA / PMN Number
K040676
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

FAILURE ANALYSIS REVEALED THAT THE INSULIN PUMP WAS UNABLE TO PRIME DURING THE PRIME TEST AS A RESULT OF A LOOSE DRIVE SUPPORT DISK.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CUSTOMER'S INSULIN PUMP ALARMED AN ERROR. NO FURTHER INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PARADIGM INSULIN INFUSION PUMP LZG LZG MEDTRONIC PUERTO RICO OPERATIONS CO. MMT-715WWL

Patients

Seq Age Sex Outcome Treatment
1