Meridian Bioscience recalls specific lot of ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) due to improper storage temperature. This may affect test accuracy but does not pose immediate safety risks.
A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.
Meridian Bioscience is recalling a specific lot of ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) because they were stored at incorrect temperatures in warehouses. This could lead to inaccurate test results but does not pose a direct safety hazard.
The test kits were stored at temperatures outside the labeled requirements in Medline warehouses. This improper storage could cause the test kits to become less accurate or ineffective when used. However, the hazard does not involve physical harm or immediate safety risks.
Users of the Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) who purchased the specific lot number 08241275 are affected. Laboratory or home users performing these tests may be at risk of inaccurate results.
Check for the model number 750830 on the test kit packaging. The specific lot number 08241275 is affected. This lot was stored improperly in Medline warehouses.
Verify the model number (750830) and lot number (08241275) on the test kit packaging.
The specific lot of test kits was stored at incorrect temperatures in Medline warehouses, which could affect test accuracy.
No, this recall does not pose a safety risk. The issue is related to test accuracy, not physical harm.
Check the model number (750830) and lot number (08241275) on the test kit packaging.
We’ve drafted a message you can send Meridian Bioscience to request your refund or repair — edit it as you like.
Subject: Recall Z-1719-2025 — Meridian Bioscience Meridian Bioscience Hello, I own a Meridian Bioscience that is covered by recall Z-1719-2025 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.
