FDA Adverse Event Malfunction Summary report: N

OT ULTRALINK METER

MDR report key: 2823147 · Received November 7, 2012

Report

Report Number
2939301-2012-12885
Event Type
Malfunction
Date Received
November 7, 2012
Report Date
October 28, 2012
Manufacturer
LIFESCAN INC.
Product Code
NBW
PMA / PMN Number
K073231
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT IS EXPECTED TO BE RETURNED.

Description of Event or Problem · 1

THERE IS NO INDICATION THAT THE PRODUCT CAUSED OR CONTRIBUTED TO AN ADVERSE EVENT. HOWEVER, THIS COMPLAINT IS BEING REPORTED BECAUSE ERROR 5 METER ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OT ULTRALINK METER GLUCOSE MONITORING SYS/KIT NBW LIFESCAN INC. 3234477

Patients

Seq Age Sex Outcome Treatment
1 106 YR