FDA Adverse Event Malfunction Summary report: N

FREESTYLE FLASH

MDR report key: 1021393 · Received May 29, 2007

Report

Report Number
2954323-2007-09009
Event Type
Malfunction
Date Received
May 29, 2007
Date of Event
April 30, 2007
Report Date
May 29, 2007
Manufacturer
ABBOTT DIABETES CARE INC, USA
Product Code
LFR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE METER HAS BEEN CONFIRMED TO EXHIBIT THE MEMORY OVERWRITE MALFUNCTION. CUSTOMERS AND RETAILERS HAVE BEEN INFORMED.

Description of Event or Problem · 1

A CUSTOMER REPORTED AN ISSUE WITH THEIR FREESTYLE FLASH METER. UPON PRODUCT INVESTIGATION, IT WAS DISCOVERED THE METER EXHIBITED THE MEMORY OVERWRITE MALFUNCTION. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FREESTYLE FLASH BLOOD GLUCOSE MONITORING SYSTEM LFR ABBOTT DIABETES CARE INC, USA NA 0503532

Patients

Seq Age Sex Outcome Treatment
1 UNK