FDA Adverse Event Malfunction Summary report: N

TRIAGE PROFILER SOB PANEL

MDR report key: 9226694 · Received October 23, 2019

Report

Report Number
3013982035-2019-00028
Event Type
Malfunction
Date Received
October 23, 2019
Date of Event
September 22, 2019
Report Date
September 23, 2019
Manufacturer
QUIDEL CARDIOVASCULAR INC.
Product Code
MMI
PMA / PMN Number
K080269
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LE
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION CONCLUSION: THE CUSTOMERS COMPLAINT WAS NOT REPLICATED WITH IN-HOUSE TESTING OF RETAIN LOT T10226B. NO ISSUES WITH TNI RECOVERY WERE OBSERVED. MANUFACTURING BATCH RECORDS FOR LOT T10226B 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 CORRECTIVE ACTION IS REQUIRED. ALTHOUGH THIS CATALOG NUMBER (97300EU) IS NOT APPROVED IN THE UNITED STATES, THIS EVENT IS BEING REPORTED AS THE DEVICE IS SAME/SIMILAR TO CATALOG NUMBER 97300, 510(K) NUMBER K080269. .

Description of Event or Problem · 1

CUSTOMER REPORTED DISCORDANT TROPONINI RESULTS BETWEEN TRIAGE AND MINIVIDAS. (B)(6) MALE TESTED ON TRIAGE AND PRODUCED THE FOLLOWING RESULTS: CKMB: 2.2NG/ML, MYO: 283NG/ML, TNI: 0.15NG/ML, BNP: 1040PG/ML, D-DIMER: 2050NG/ML. A SEPARATE SAMPLE, DRAWN AT THE SAME TIME AS TRIAGE SAMPLE WAS TESTED ON MINIVIDAS AND RESULTED = 1070.7NG/L. CUSTOMER STATED PATIENT WAS ADMITTED FOR MI AND UNDERWENT CARDIAC CATHETERIZATION. MINIVIDAS CUT-OFF: MALE IS >25NG/L. TRIAGE SOB TROPONIN CUT-OFF: 0.40 NG/ML. CUSTOMER STATED THE PATIENT WAS UNAFFECTED BY THE TRIAGE RESULTS BECAUSE TRIAGE WAS STILL IN EVALUATION PHASE. CUSTOMER USED MINIVIDAS FOR THEIR CLINICAL DECISION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1020029 TRIAGE PROFILER SOB PANEL TRIAGE SOB PANEL MMI QUIDEL CARDIOVASCULAR INC. 97300EU T10226B

Patients

Seq Age Sex Outcome Treatment
1 63 YR