FDA Adverse Event Malfunction Summary report: N

TRIAGE CARDIAC TRIPLE MARKER PANEL

MDR report key: 6122130 · Received November 22, 2016

Report

Report Number
2027969-2016-00691
Event Type
Malfunction
Date Received
November 22, 2016
Date of Event
October 20, 2016
Report Date
October 25, 2016
Manufacturer
ALERE SAN DIEGO, INC.
Product Code
NBC
PMA / PMN Number
K030286
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SD, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION CONCLUSION: INVESTIGATION PENDING.

Additional Manufacturer Narrative · 1

INVESTIGATION/CONCLUSION: ONE LOW TNI RESULT WAS OBSERVED DURING IN-HOUSE TESTING OF RETAINED DEVICE LOT W62028. ALTHOUGH THE CUSTOMER'S COMPLAINT WAS REPLICATED, THE TNI TOTAL CV WAS FOUND TO BE WITHIN THE PACKAGE INSERT CLAIM. THE METER ASSOCIATED WITH THE COMPLAINT WAS RETURNED FOR INVESTIGATION. IN-HOUSE TESTING OF THE RETURNED METER DID NOT REPLICATE THE CUSTOMER'S COMPLAINT. NO ISSUES WERE OBSERVED. MANUFACTURING BATCH RECORDS FOR LOT W62028 WERE REVIEWED AND FOUND THAT THE LOT MET RELEASE SPECIFICATIONS. FURTHER INVESTIGATION WILL NOT BE PURSUED AS THE CUSTOMER'S REPORTED TRIAGE AND REFERENCE RESULTS ALL HAD THE SAME CLINICAL OUTCOME. PRODUCT DEFICIENCY WAS NOT ESTABLISHED.

Description of Event or Problem · 1

REPORT RECEIVED OF DISCREPANT LOW TNI 2X ON 1 METER/1 LOT. PATIENT #1 TRIAGE=3.98; VISTA DIMENSION=7.84, 8.03/ CONTROLS AND QCD PASS. THREE HOURS BETWEEN CORRELATIONS. REFERENCE RANGE FOR VISTA DIMENSION: 0-0.05. STD DEVIATION FOR VISTA DIMENSION: 0.004; CV=0.05 . TESTING FOR TNI ON BOTH INSTRUMENTS. NO SPECIFIC PATIENT INFORMATION PROVIDED. NO REPORTED ADVERSE PATIENT SEQUELA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
770886 TRIAGE CARDIAC TRIPLE MARKER PANEL CARDIAC MARKER TEST NBC ALERE SAN DIEGO, INC. 97000HS W62028B

Patients

Seq Age Sex Outcome Treatment
1 TRIAGE METERPRO DOMESTIC KIT SERIAL #(B)(4)