Abbott recalls ARC T-Uptake Assay reagents due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected units.
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 is recalling ARC T-Upt:ake Assay reagents because thunderstorms caused some shipments to be stored outside recommended conditions. This could lead to incorrect or delayed test results if the reagents are used.
Thunderstorms caused transit delays for some reagent shipments, leading to improper storage conditions. This could result in incorrect or delayed test results if the reagents are used after being stored outside recommended conditions.
Healthcare facilities using Abbott ARC T-Uptake Assay reagents may be affected. Those using the reagents for critical tests are at higher risk if improper storage occurred.
Check for the product name 'ARC T-Uptake Assay (100TST/BX) ABBDIA REAGENT' with catalog number 02K4825 or GTIN 380740003517. The reagents were sold through Mckesson Medical-Surgical.
Verify the product name, catalog number, and GTIN to confirm if your reagent is affected.
Thunderstorms caused transit delays for some shipments, leading to improper storage conditions that could cause incorrect or delayed test results.
Check for the product name 'ARC T-Uptake Assay (100TST/BX) ABBDIA REAGENT' with catalog number 02K4825 or GTIN 380740003517.
The recall does not require immediate action; check product details to confirm if your reagent is affected.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1844-2025 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1844-2025 from Abbott. 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.
