FDA Adverse Event Malfunction Summary report: N

ID NOW COVID-19

MDR report key: 12321590 · Received August 13, 2021

Report

Report Number
1221359-2021-02262
Event Type
Malfunction
Date Received
August 13, 2021
Report Date
August 13, 2021
Manufacturer
ABBOTT DIAGNOSTICS SCABOROUGH
Product Code
QJR
UDI-DI
10811877011320
PMA / PMN Number
EUA2000074
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION: TESTING WAS PERFORMED AT ABBOTT DIAGNOSTICS (B)(4), INC. ON RETAINED KIT LOT M140253 WITH INTERNAL POSITIVE QUALITY CONTROL SAMPLES AND NEGATIVE QUALITY CONTROL SWABS. ALL TEST RESULTS WERE VALID AND PERFORMED AS EXPECTED. ADDITIONALLY, THE MANUFACTURING RECORDS AND QUALITY CONTROL RELEASE TESTING WAS REVIEWED FOR TEST KIT TEST BASE PART NUMBER 190-430 / LOT M140253. THE LOT MET THE REQUIRED RELEASE SPECIFICATIONS. A REVIEW OF THE COMPLAINTS REPORTED AS FALSE POSITIVE PATIENT RESULTS (CONFIRMED AND UNCONFIRMED, CONFLICTING RESULTS) RELATED TO KIT LOT (B)(6) ABBOTT DIAGNOSTICS (B)(4) WAS UNABLE TO DETERMINE THE EXACT ROOT CAUSE OF THE REPORTED ISSUE HOWEVER A POSSIBLE ASSIGNABLE ROOT CAUSE IS SAMPLE INTERFERENCE OR CROSS CONTAMINATION. THIS EVENT WAS ORIGINALLY REPORTED IN MDR FOLLOW UP # 1 1221359-2021-01872. REFERENCE MFR NUMBERS: 1221359-2021-01877, 1221359-2021-02260, 1221359-2021-02261.

Description of Event or Problem · 0

THE CUSTOMER REPORTED A DISCREPANT POSITIVE TEST RESULT WHILE USING THE ID NOW COVID-19 ASSAY ON A PATIENT THAT PRESENTED TO THE EMERGENCY ROOM. PCR CONFIRMATION TESTING GENERATED A NEGATIVE RESULT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1214917 ID NOW COVID-19 MOLECULAR IVD FOR ID NOW COVID-19 QJR ABBOTT DIAGNOSTICS SCABOROUGH M140253 10811877011320

Patients

Seq Age Sex Outcome Treatment
1