FDA Adverse Event Malfunction Summary report: N

ONE TOUCH ULTRA

MDR report key: 660510 · Received January 3, 2006

Report

Report Number
2939301-2006-00002
Event Type
Malfunction
Date Received
January 3, 2006
Report Date
December 27, 2005
Manufacturer
LIFESCAN, INC.
Product Code
NBW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

A PATIENT REPORTED BLOOD GLUCOSE RESULTS OF "141, 227, AND 553 MG/DL" WITH A LIFESCAN METER, PERFORMED WITHIN 10 MINUTES OF EACH OTHER. THE CONTROL SOLUTION WAS REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ONE TOUCH ULTRA GLUCOSE MONITORING SYS/KIT NBW LIFESCAN, INC. NA 2604545

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN