FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK COMFORT CURVE TEST STRIPS

MDR report key: 1040984 · Received May 8, 2008

Report

Report Number
1823260-2008-03860
Event Type
Malfunction
Date Received
May 8, 2008
Date of Event
April 23, 2008
Report Date
May 8, 2008
Manufacturer
ROCHE DIAGNOSTICS
Product Code
LFR
PMA / PMN Number
K010362
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
LAY USER/PATIENT

Narratives

Description of Event or Problem · 1

CUSTOMER REPORTS BACK TO BACK TESTING ON THE SAME METER WHILE USING THE ADVANTAGE SYS WITH RESULTS OF 180 OR 199 MG/DL AND 98 OR 102 MG/DL. NO QUALITY CONTROLS WERE RUN. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR RETURN OF THE SUSPECT PROD AND A REPLACEMENT WAS SENT.

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 550080

Patients

Seq Age Sex Outcome Treatment
1 74 YR ATENOLOL 50 MG/DAY| LISINOPRIL 20 MG/DAY| NIFEDICAL 60 MG/DAY| METFORMIN 500 MG/DAY