FDA Adverse Event Malfunction Summary report: N

TRIAGE CARDIAC HS TNI PANEL

MDR report key: 11904887 · Received May 28, 2021

Report

Report Number
3013982035-2021-00009
Event Type
Malfunction
Date Received
May 28, 2021
Report Date
April 29, 2021
Manufacturer
QUIDEL CARDIOVASCULAR INC.
Product Code
MMI
PMA / PMN Number
K030286
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION CONCLUSION: THE CUSTOMERS COMPLAINT WAS NOT REPLICATED DURING IN-HOUSE TESTING OF RETAIN DEVICE LOT T11864RN. RETAINS OF THE COMPLAINT LOT PERFORMED PROPERLY WHEN TESTED WITH A LOW LEVEL POSITIVE TNI CALIBRATOR, NO RESULTS <0.05NG/ML. MANUFACTURING BATCH RECORDS FOR LOT T11864RN WERE REVIEWED AND FOUND THAT THE LOT MET FINAL RELEASE SPECIFICATIONS. BASED ON THE INFORMATION AVAILABLE, THERE IS NO INDICATION OF A PRODUCT DEFICIENCY AND NO CORRECTION ACTION IS REQUIRED.

Description of Event or Problem · 0

CUSTOMER REPORTED DISCREPANCIES IN CORRELATION BETWEEN NEW TRIAGE METER AND ECI/VITROS. ECI 0.063. TRIAGE <0.05 . ECI 0.068, TRIAGE <0.05 . ECI 0.082, TRIAGE <0.05. ECI 0.096, TRIAGE <0.05. CUSTOMER USING TWO LOTS OF TRIAGE DEVICES. THIS MDR IS FOR TRIAGE LOT T11864RN. MDR 3013982035-2021-00010 WILL BE FILED FOR LOT T11876N. SITE CUT-OFF FOR ECI >0.012. SITE CUT-OFF FOR TRIAGE >0.05. CUSTOMER STATED NO MEDICAL DECISION WERE MADE ON TRIAGE RESULTS. THE TRIAGE METER IS NOT BEING USED FOR PATIENT RESULTS, THEY ARE ATTEMPTING TO PERFORM A VALIDATION TO IMPLEMENT THE METER. NO ADDITIONAL PATIENT INFORMATION COULD BE PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
800898 TRIAGE CARDIAC HS TNI PANEL TRIAGE CARDIAC HS TNI PANEL MMI QUIDEL CARDIOVASCULAR INC. 97021HS T11864RN

Patients

Seq Age Sex Outcome Treatment
1 TRIAGE METERPRO, PN: 55070, SN: (B)(4)