FDA Adverse Event Injury Summary report: N

DIASORIN LIASON XL HSV 1

MDR report key: 16807772 · Received April 24, 2023

Report

Report Number
MW5116972
Event Type
Injury
Date Received
April 24, 2023
Date of Event
December 27, 2022
Report Date
April 19, 2023
Manufacturer
DIASORIN INC.
Product Code
MXJ
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
117
Health Professional
Yes

Narratives

Description of Event or Problem · 0

PATIENT HAD A HSV 2 POSITIVE TEST ON THE DIASORIN HSV 1 AND 2 IGG TEST, FOLLOWED UP WITH A WESTERN BLOT WHICH WAS NEGATIVE FOR HSV 2. DATE GIVEN IS THE WESTERN BLOT CONFIRMATORY TEST. REFERENCE REPORT: MW5116973.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1612785 DIASORIN LIASON XL HSV 1 ENZYME LINKED IMMUNOSORBENT ASSAY, HERPES SIMPLEX VIRUS, HSV-1 MXJ DIASORIN INC.

Patients

Seq Age Sex Outcome Treatment
1 29 YR Male Other