FDA Adverse Event Death Summary report: N

PUMP, INSULIN, 512 NA BLUE

MDR report key: 555161 · Received November 16, 2004

Report

Report Number
2032227-2004-02138
Event Type
Death
Date Received
November 16, 2004
Date of Event
October 26, 2004
Report Date
October 26, 2004
Manufacturer
MEDTRONIC MINIMED
Product Code
LZG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
INVALID DATA

Narratives

Description of Event or Problem · 1

THEY CALLED TO REPORT CUSTOMER PASSED AWAY IN 12/2003 DUE TO A CAR ACCIDENT. THEY STATED CUSTOMER WAS WEARING THE PUMP AT THE TIME OF ACCIDENT. THEY ALSO STATES CUSTOMER DID NOT HAVE THEIR SEAT BELT ON; THEY DONATED THE PUMP TO HOSPITAL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PUMP, INSULIN, 512 NA BLUE INFUSION PUMP LZG MEDTRONIC MINIMED MMT-512NAB *

Patients

Seq Age Sex Outcome Treatment
1 47 YR Death