FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK COMFORT CURVE TEST STRIPS

MDR report key: 854227 · Received March 5, 2007

Report

Report Number
1823260-2007-01840
Event Type
Malfunction
Date Received
March 5, 2007
Date of Event
January 15, 2007
Report Date
March 5, 2007
Manufacturer
ROCHE DIAGNOSTICS
Product Code
LFR
PMA / PMN Number
K010362
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

SUSPECT DEVICE: COMFORT CURVE TEST STRIPS.

Description of Event or Problem · 1

CUSTOMER REPORTEDLY OBTAINED RESULTS OF 600MG/DL, 105MG/DL AND 108MG/DL WITHIN 10 MINUTES ON THE ADVANTAGE TEST SYSTEM. NO ACTION TAKEN BASED ON DEVICE RESULTS. NO ADVERSE EVENT REPORTED. REQUESTED RETURN OF SUSPECT TEST SYSTEM AND REPLACEMENT WAS SENT. NO INFORMATION PROVIDED FOR WHERE COMPARISON OCCURRED. NO QUALITY CONTROLS WERE USED. ADVANTAGE TEST SYSTEM: STRIP LOT 549527, EXP 2/29/08, CAT/2030381.

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 * 549527

Patients

Seq Age Sex Outcome Treatment
1 NA