Abbott Diagnostics recalls 100-test progestrone reagent due to transit delays causing improper storage. This may lead to incorrect or delayed test results. Affected units have specific catalog and order numbers.
transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
Abbott Diagnostics is recalling its Architect Progestrone reagent (100 tests) because severe thunderstorms caused transit delays, potentially leading to improper storage. This could result in incorrect or delayed test results if the reagent is used after the recall.
Severe thunderstorms caused transit delays for the reagent, leading to improper storage conditions. This could increase the chance of incorrect or delayed test results if the reagent is used after the recall.
Healthcare providers using the Abbott Architect Progestrone reagent for hormone testing are likely affected. Those who have the specific catalog number 07K7725 or order number 46048552 are most at risk.
Check for the catalog number 07K7725 or order number 46048552 on the reagent packaging. The product is sold under the Abbott Diagnostics Architect Progestrone (100 tests) name.
Verify the catalog number 07K7725 or order number 46048552 on the reagent packaging.
Severe thunderstorms caused transit delays, leading to improper storage conditions that could increase the chance of incorrect or delayed test results.
Check the catalog number 07K7725 or order number 46048552 on the packaging to confirm if it's affected. No action is required if it's not the specific model.
The recall does not provide a fix; affected units should be checked for the specific catalog and order numbers.
We’ve drafted a message you can send Abbott Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1851-2025 — Abbott Diagnostics Abbott Diagnostics Hello, I own a Abbott Diagnostics that is covered by recall Z-1851-2025 from Abbott Diagnostics. 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.
