FDA Adverse Event Malfunction Summary report: N

TRIAGE CARDIAC TNI PANEL

MDR report key: 20163228 · Received September 6, 2024

Report

Report Number
3013982035-2024-00017
Event Type
Malfunction
Date Received
September 6, 2024
Date of Event
August 2, 2024
Report Date
September 6, 2024
Manufacturer
QUIDEL CARDIOVASCULAR INC.
Product Code
MMI
PMA / PMN Number
K030286
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

UNABLE TO DETERMINE THE ROOT CAUSE OF THE DISCREPANT HIGH TNI OBSERVATION. IN-HOUSE TESTING ILLUSTRATED THAT THE PRODUCT IS PERFORMING AS EXPECTED RELATIVE TO THE COMPLAINT AND THE DATA HAS BEEN DETERMINED TO BE ACCEPTABLE ACCORDING TO THE RISK STATEMENT. ALTHOUGH AN EXACT ROOT CAUSE HAS NOT BEEN DETERMINED, THE ISSUE WAS NOT REPEATED WITH ADDITIONAL TESTING, AND APPEARS TO BE AN ISOLATED EVENT. BASED ON THE INFORMATION AVAILABLE, THERE IS NO INDICATION OF A PRODUCT DEFICIENCY AND NO CORRECTIVE ACTION IS REQUIRED.

Additional Manufacturer Narrative · 0

INVESTIGATION INTO THIS ISSUE IS ONGOING.

Description of Event or Problem · 0

CUSTOMER REPORTED THAT THERE HAVE BEEN 2 PATIENTS WHO RECEIVED HIGHER THAN EXPECTED TNI RESULTS AND UPON REPEAT, A NORMAL EXPECTED RESULT WAS OBTAINED. NO CONFIRMATORY TESTING WAS CONDUCTED, NO OTHER ABNORMAL LABS WERE OBTAINED. THE PATIENTS MATCHED THE CLINICAL SYMPTOMS OF THE NORMAL RESULTS. THE PATIENTS WERE RELEASED FROM THE EMERGENCY DEPARTMENT AND SENT HOME. ALTHOUGH REQUESTED, NO ADDITIONAL INFORMATION WAS PROVIDED. THIS IS REPORT 1 OF 2.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1360616 TRIAGE CARDIAC TNI PANEL TRIAGE CARDIAC TNI PANEL MMI QUIDEL CARDIOVASCULAR INC. 97021HS T14913RN

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown TRIAGE METERPRO PN:55070 SN: (B)(6)