FDA Adverse Event Malfunction Summary report: N

ARCHITECT TOTAL B-HCG REAGENT KIT

MDR report key: 16751137 · Received April 17, 2023

Report

Report Number
3005094123-2023-00102
Event Type
Malfunction
Date Received
April 17, 2023
Date of Event
March 28, 2023
Report Date
May 9, 2023
Manufacturer
ABBOTT IRELAND DIAGNOSTICS DIVISION
Product Code
DHA
PMA / PMN Number
K983424
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TU
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

RETURN TESTING WAS NOT COMPLETED AS RETURNS WERE NOT AVAILABLE. MANUFACTURING DOCUMENTATION FOR THE LIKELY CAUSE LOT DID NOT IDENTIFY ANY ISSUES ASSOCIATED WITH THE COMPLAINT ISSUE. THE TICKET SEARCH DETERMINED THAT THERE IS NORMAL COMPLAINT ACTIVITY FOR THIS LOT NUMBER AND THERE ARE NO TRENDS FOR THE PRODUCT RELATED TO PATIENT RESULTS. THE OVERALL PERFORMANCE OF ARCHITECT TOTAL SS-HCG REAGENTS IN THE FIELD WAS REVIEWED USING DATA GATHERED VIA ABBOTTLINK FROM CUSTOMERS WORLDWIDE. THE NUMBER OF STANDARD DEVIATIONS TO THE CUT-OFF AND THE MEDIAN OF THE NEGATIVE POPULATIONS IS WITHIN THE ESTABLISHED LIMITS AND WITHIN THE HISTORICAL RANGE OF THE ARCHITECT TOTAL B-HCG ASSAY. A REVIEW OF THE PRODUCT LABELING CONCLUDED THAT THE ISSUE IS SUFFICIENTLY ADDRESSED. BASED ON THE INVESTIGATION NO SYSTEMIC ISSUE OR PRODUCT DEFICIENCY WAS IDENTIFIED FOR THE ARCHITECT TOTAL B-HCG LOT# 42344UD00.

Additional Manufacturer Narrative · 0

AN EVALUATION IS IN PROCESS. A FOLLOW UP REPORT WILL BE SUBMITTED WHEN THE EVALUATION IS COMPLETE.

Description of Event or Problem · 0

THE CUSTOMER REPORTED A FALSE POSITIVE ARCHITECT TOTAL B-HCG RESULT ON A 36-YR OLD FEMALE PATIENT THAT WAS REPORTED OUT OF THE LABORATORY. RESULTS PROVIDED: 28MAR2023 SID (B)(6) = 474.00 MIU/ML, REPEATED ON 29MAR2023 SID 124067 = < 1.20 MIU/ML. NO IMPACT TO PATIENT MANAGEMENT WAS REPORTED.

Description of Event or Problem · 0

THE CUSTOMER REPORTED A FALSE POSITIVE ARCHITECT TOTAL B-HCG RESULT ON A 36-YR OLD FEMALE PATIENT THAT WAS REPORTED OUT OF THE LABORATORY. RESULTS PROVIDED: (B)(6) 2023 SID 1241709 = 474.00 MIU/ML, REPEATED ON (B)(6) 2023 SID 124067 = < 1.20 MIU/ML. NO IMPACT TO PATIENT MANAGEMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1818439 ARCHITECT TOTAL B-HCG REAGENT KIT SYSTEM, TEST, HUMAN CHORIONIC GONADOTROPIN DHA ABBOTT IRELAND DIAGNOSTICS DIVISION 7K78-35 42344UD00

Patients

Seq Age Sex Outcome Treatment
1 36 YR Female ARC I2K PROC MOD, 03M74-01, ISR03493| ARC I2K PROC MOD, 03M74-01, ISR03493