FDA Adverse Event Malfunction Summary report: N

INRATIO

MDR report key: 1692619 · Received May 13, 2010

Report

Report Number
2027969-2010-00578
Event Type
Malfunction
Date Received
May 13, 2010
Date of Event
March 16, 2010
Report Date
May 13, 2010
Manufacturer
BIOSITE INCORPORATED
Product Code
JPA
PMA / PMN Number
K021923
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

DISCREPANT RESULTS (ACCURACY). COMPARISON OF INRATIO TEST WITH LAB RESULTS PROVIDED BY END-USER AT TIME COMPLAINT WAS FILED: SEE SCANNED TABLE. THREE HRS IS CONSIDERED A REASONABLE LENGTH OF TIME BETWEEN TWO READINGS IN ORDER FOR COMPARISON TO BE VALID. THE MEAN OF THE INRATIO METER AND COMPARATIVE SYSTEM INR WERE CALCULATED. BOTH INRATIO AND REFERENCE VALUES ARE WITHIN THE CONFIDENCE LIMITS FOR INR TESTING. TEST 7 HAS A VALUE ABOVE 5.0 AND IS NOT CONSIDERED DISCREPANT WITHIN THE CONTEXT OF DOCUMENTED VARIABILITY FOR INR TESTING. INR REPORTED TO HAVE MET THE CRITERIA FOR ACCURACY. NO FURTHER INVESTIGATION WILL BE PURSUED. METER INVESTIGATION: UNIT WAS TESTED WITH THERMOMETER SENSING TEST DURING WARM UP TO DETERMINE IF UNIT'S HEATER PLATE IS WITHIN THE STANDARD SPECIFICATION (36.00-38.00 DEGREES CELSIUS). PERFORMED THERMOMETER SENSING TEST ON UNIT AND BOTH THERMISTOR ARE MEASURED AS FOLLOWS: THERMISTOR #1 = 36.00 DEGREES CELSIUS THERMISTOR #2 = 36.19 DEGREES CELSIUS. VISUAL INSPECTION REVEALED SIGNIFICANT CONTAMINATION ON HEATER PLATE, BUT IT HAS NOT AFFECTED THE PERFORMANCE OF THE TEMP CONTROL UNIT. METER FUNCTIONAL TEST PLAN WAS PERFORMED AND ALL TESTS WERE COMPLETED WITH "PASS". STRIP LOT# 080584A EXPIRED ON THE LAST DAY OF SEPT 2009. STRIP LOT USED WAS EXPIRED: TRENDING NOT REQUIRED. CORRECTIVE ACTION NOT REQUIRED AT THIS TIME.

Description of Event or Problem · 1

CALLER ALLEGED DISCREPANT RESULTS COMPARED WITH THE LAB. RESULTS AS FOLLOWS: INRATIO: 1.0, INRATIO: 1.0, INRATIO: 1.0. TESTS WERE FROM A NURSING ADMINISTRATION TEST STUDY: ONE PT, PERFORMED AT DIFFERENT TIMES. TEST 3 USED STRIP CODE 066KH. TEST 1 AND 2 USED STRIP LOT # 222166. STUDY PERFORMED WITH (3) PT'S OVER (7) DAYS. PT INFO WAS NOT GIVEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INRATIO PROTHROMBIN TIME TEST JPA BIOSITE INCORPORATED 100139 080584A

Patients

Seq Age Sex Outcome Treatment
1