FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK COMFORT CURVE TEST STRIPS

MDR report key: 1170819 · Received September 15, 2008

Report

Report Number
1823260-2008-06905
Event Type
Malfunction
Date Received
September 15, 2008
Date of Event
September 5, 2008
Report Date
September 15, 2008
Manufacturer
ROCHE DIAGNOSTICS
Product Code
LFR
PMA / PMN Number
K010362
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Additional Manufacturer Narrative · 1

THE MEDWATCH IS FOR THE SUSPECT DEVICE USED IN ADVANTAGE SYSTEM #2. PLEASE SEE MEDWATCH IS FOR SUSPECT DEVICE IN ADVANTAGE SYSTEM #1.

Description of Event or Problem · 1

CALLER REPORTS BACK TO BACK RESULTS OF 302MG/DL ON ADVANTAGE SYSTEM #1 COMPARED TO RESULTS OF 89MG/DL ON ADVANTAGE SYSTEM #2. NO QUALITY CONTROLS WERE RUN ON SYSTEM #2. NO ADVERSE EVENT REPORTED. A REQUEST WAS MADE FOR RETURN OF THE SUSPECT PRODUCT 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 550775

Patients

Seq Age Sex Outcome Treatment
1 83 YR TRAZODONE -"A NUMBER OF YRS"| LEVOTHYROXINE - OVER 1 YR| FUROSEMIDE -"A NUMBER OF YRS"| POTASSIUM -"A NUMBER OF YRS"| PREDNISONE - ABOUT 3 YRS| CAPTOPRIL - ABOUT 2 YRS| ZOCOR -"A NUMBER OF YRS"| GLYBURIDE 2-3 YRS| OXYCODONE - 2-3 YRS| MEXITIL ABOUT 6 MONTHS| BISOPROLOL ABOUT 6 MONTHS| SPRONOLACTONE - 6 MONTHS TO A YR| CELEXA - UNK| ASPIRIN -"A NUMBER OF YRS"