Medline Industries recalls Meridian Bioscience Immunocard STAT! Rotavirus tests due to being shipped at room temperature instead of refrigerated. This could lead to inaccurate test results.
The product was incorrectly shipped at room temperature rather than refrigerated.
Medline Industries is recalling Meridian Bioscience Immunocard STAT! Rotavirus tests that were shipped at room temperature instead of refrigerated. This could cause inaccurate test results, especially if used for diagnosing rotavirus infections.
The tests were shipped at room temperature instead of refrigerated, which could cause the test to become less effective. This might lead to inaccurate results when used for diagnosing rotavirus infections.
People who own or use the Meridian Bioscience Immunocard STAT! Rotavirus tests with lot numbers 750030M481, 750030N482, or 750030N483 are affected. Those using the tests for rotavirus diagnosis are most at risk of inaccurate results.
Check the lot number on the test kit box. The affected lots are 750030M481 (expires 4/29/2022), 750030N482 (expires 12/2/2022), and 750030N483 (expires 5/17/2023).
Look for the lot number on the test kit box to determine if it's affected.
The tests were shipped at room temperature instead of refrigerated, which could cause inaccurate results.
Check the lot number on the test kit box. If it's one of the affected lots (750030M481, 750030N482, or 750030N483), you may want to contact Medline Industries for further instructions.
The tests may not work correctly if they were shipped at room temperature instead of refrigerated, leading to inaccurate results for rotavirus diagnosis.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0678-2022 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0678-2022 from Medline Industries. 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.
