FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK COMFORT CURVE TEST STRIPS

MDR report key: 1032701 · Received April 22, 2008

Report

Report Number
1823260-2008-03436
Event Type
Malfunction
Date Received
April 22, 2008
Date of Event
April 5, 2008
Report Date
April 22, 2008
Manufacturer
ROCHE DIAGNOSTICS
Product Code
LFR
PMA / PMN Number
K010362
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
LAY USER/PATIENT

Narratives

Description of Event or Problem · 1

THE REPORTER STATES THAT SHE OBTAINED BLOOD GLUCOSE COMPARISON WITH RESULTS 97MG/DL, 140MG/DL, 298MG/DL AND 110MG/DL ON THE ACCU-CHEK ADVANTAGE SYSTEM. THE RESULTS WERE OBTAINED WITHIN A 10 MIN TIMEFRAME. SHE TREATED HERSELF AND FELT BETTER AFTER TREATMENT. NO ADVERSE EVENT REPORTED. NEW SYSTEM SENT TO CUSTOMER AND RETURN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACCU-CHEK COMFORT CURVE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS - LFR LFR ROCHE DIAGNOSTICS 550500

Patients

Seq Age Sex Outcome Treatment
1 54 YR APIDRA SLIDING SCALE 1.5 MONTHS| LEVEMIR "50-55 UNITS/DAY" 1.5 MONTHS