Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recall: Storage Temperature
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/52545-meridian-bioscience-immunocard-stat-crypto-giardia-test-kits-recall-storage.
Source Summary by GovInfoNow · govinfonow.com/recall/52545-meridian-bioscience-immunocard-stat-crypto-giardia-test-kits-recall-storage · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1719-2025
Cite this page
“Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recall: Storage Temperature.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52545-meridian-bioscience-immunocard-stat-crypto-giardia-test-kits-recall-storage. Based on FDA recall #Z-1719-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1719-2025%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Meridian Bioscience- Category
Medical device
What to do — step by step
Check Product Details
Verify the model number (750830) and lot number (08241275) on the test kit packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 51 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-1719-2025 (March 24, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1719-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.