Diasorin recalls specific lots of HSV-2 Type Specific IgG test kits that may produce false positive results. Affected lots include 136344 through 136775. No action needed for users but verify your lot number.
DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520, 136520A, 136520B, 136520C, 136604, 136703, 136703A, 136703B, 136703C 136775of LIAISON HSV-2 Type Specific IgG assay may produce increased equivocal and/or false positive results.
Diasorin is recalling certain lots of HSV-2 Type Specific IgG test kits that may give false positive results. This could lead to incorrect diagnoses of herpes simplex virus type 2. No action is required for users but they should check their lot numbers.
The recalled test kits may produce increased equivocal or false positive results, meaning they could incorrectly indicate herpes simplex virus type 2 infection when none exists. This might lead to unnecessary anxiety or treatment decisions.
People who use the DiaSorin LIAISON HSV-2 Type Specific IgG test kits with lot numbers 136344 through 136775. Those most at risk are individuals who rely on these tests for herpes diagnosis.
Check the lot number on your test kit, which should be one of 136344, 136344A, 136344B, 136344C, 136520, 136520A, 136520B, 136520C, 136604, 136703, 136703A, 136703B, 136703C, or 136775.
Look for the lot number on your test kit, which should be one of the listed numbers.
No action is needed. The recall is for verification only; users should check their lot numbers.
It means the test may incorrectly indicate herpes simplex virus type 2 infection when none exists, leading to unnecessary concern or treatment.
Check the lot number on your test kit; affected lots are 136344 through 136775.
We’ve drafted a message you can send Diasorin to request your refund or repair — edit it as you like.
Subject: Recall Z-0815-2024 — Diasorin Diasorin Hello, I own a Diasorin that is covered by recall Z-0815-2024 from Diasorin. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
