Meridian Bioscience recalls Revogene SARS-CoV-2 test kits with potential specimen leakage, risking lab exposure to SARS-CoV-2. Affected lots include 410700P019 to 410700P024 and 410700P027.
Leakage of the original specimen from the plastic microfluidic cartridge (PIE), possibility that laboratory personnel may be exposed to aerosolized specimen containing SARS-CoV-2
Meridian Bioscience is recalling Revogene SARS-CoV-2 test kits due to a risk of specimen leakage that could expose lab personnel to SARS-CoV-2. This recall affects specific lot numbers of the test kits used in laboratories.
The test kits can leak original specimens from the plastic cartridge, potentially creating aerosols that contain SARS-CoV-2. This poses a risk of laboratory exposure to the virus if proper safety protocols aren't followed.
Laboratory personnel using the Revogene SARS-CoV-2 test kits with affected lot numbers are most at risk. The recall applies to specific batches sold to labs.
Check the lot number on the test kit packaging. Affected lots are 410700P019 through 410700P024 and 410700P027.
Look for the lot number on the test kit packaging to determine if it is affected (410700P019 to 410700P024 or 410700P027).
The test kits can leak original specimens from the plastic cartridge, potentially creating aerosols that contain SARS-CoV-2, which could expose lab personnel to the virus.
Affected lot numbers are 410700P019, 410700P020, 410700P021, 410700P022, 410700P023, 410700P024, and 410700P027.
The recall does not require immediate discontinuation; laboratory personnel should check the lot number and follow proper safety protocols if using affected kits.
We’ve drafted a message you can send Meridian Bioscience to request your refund or repair — edit it as you like.
Subject: Recall Z-1008-2023 — Meridian Bioscience Meridian Bioscience Hello, I own a Meridian Bioscience that is covered by recall Z-1008-2023 from Meridian Bioscience. 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.
