FDA Adverse Event Malfunction Summary report: N

ARCHITECT STAT TROPONIN-I

MDR report key: 1374308 · Received May 6, 2009

Report

Report Number
1415939-2009-00863
Event Type
Malfunction
Date Received
May 6, 2009
Date of Event
April 14, 2009
Report Date
April 27, 2009
Manufacturer
ABBOTT LABORATORIES
Product Code
MMI
PMA / PMN Number
K041192
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
DA
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE INVESTIGATION CONSISTED OF A REVIEW OF CUSTOMER COMPLAINTS RECEIVED TO-DATE TO DETERMINE IF OTHER CUSTOMERS HAVE EXPERIENCED THE ISSUE OF ERRATIC TROPONIN-I ASSAY RESULTS. THE REVIEW OF THIS DATA DID NOT IDENTIFY ANY PROBLEMS. SPECIFICALLY, AN INCREASE IN THE NUMBER OF COMPLAINTS RELATED TO ERRATIC RESULTS WHILE USING THE REAGENT LOT NUMBER IN QUESTION OF THE ARCHITECT STAT TROPONIN-I ASSAY WERE NOT OBSERVED. THE ARCHITECT STAT TROPONIN-I PACKAGE INSERT (VERSION 840549/R6) CONTAINS SUFFICIENT INFORMATION TO ADDRESS THE CUSTOMER'S CONCERNS. PRODUCT EVALUATION TESTING IS NOT REQUIRED BECAUSE OUR REVIEW OF COMPLAINT TRACKING AND TRENDING RECORDS DID NOT FIND ANY SYSTEMIC ISSUES THAT WOULD INDICATE A POTENTIAL PRODUCT DEFICIENCY WITH THE ARCHITECT TROPONIN-I ASSAY. THE CUSTOMER'S ISSUE DOES NOT APPEAR TO BE CAUSED BY A SHIFT IN PRODUCT PERFORMANCE. THIS ASSAY IS PERFORMING ACCORDING TO ITS LABELING CLAIMS. BASED ON THE CURRENT INVESTIGATION CONDUCTED, THE ARCHITECT STAT TROPONIN-I ASSAY IS PERFORMING AS INTENDED. NO PRODUCT MALFUNCTION WAS IDENTIFIED. THIS IS A FINAL REPORT.

Additional Manufacturer Narrative · 1

THIS IS AN INITIAL REPORT. AN INVESTIGATION IS IN PROCESS. A FINAL REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETE. AN INVESTIGATION IS IN PROCESS.

Description of Event or Problem · 1

THE CUSTOMER STATES THAT ONE PATIENT SAMPLE GENERATED AN INITIAL ARCHITECT STAT TROPONIN-I ASSAY RESULT OF 0.128 UG/L (THE CUSTOMER USES A RANGE OF 0.000 - 0.030 UG/L). THE SAMPLE RETESTED AT 0.024 AND 0.023 UG/L. NO SUSPECT RESULTS WERE REPORTED FROM THE LAB. CONTROLS REMAIN WITHIN SPECIFICATIONS. THERE IS NO IMPACT TO PATIENT MANAGEMENT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ARCHITECT STAT TROPONIN-I FOR THE DETERMINATION OF CARDIAC TROPONIN-I IN HUMAN SERUM OR PLASMA MMI ABBOTT LABORATORIES 27879UN08

Patients

Seq Age Sex Outcome Treatment
1 ARCH I2000SR ANALYZER LN:3M74-01 (B)(4)| ARCH I2000SR ANALYZER LN:3M74-01 (B)(4)