FDA Adverse Event Malfunction Summary report: N

ONE TOUCH ULTRA

MDR report key: 662692 · Received January 6, 2006

Report

Report Number
2939301-2006-00097
Event Type
Malfunction
Date Received
January 6, 2006
Report Date
December 30, 2005
Manufacturer
LIFESCAN, INC.
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

A PT REPORTED BLOOD GLUCOSE RESULTS OF "102, 154, AND 110 MG/DL" WITH A LIFESCAN METER, PERFORMED WITHIN 10 MINUTES OF EACH OTHER. THE METER, TEST STRIPS, AND CONTROL SOLUTION WERE REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ONE TOUCH ULTRA GLUCOSE MONITORING SYS/KIT NBW LIFESCAN, INC. NA 2595882

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN