Abbott Diagnostics probe conditioning solution may have been stored outside recommended conditions due to thunderstorms, risking incorrect or delayed test results. Affected units include specific catalog and GTIN 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 probe conditioning solution may have been stored improperly during transit due to severe thunderstorms, which could lead to incorrect or delayed test results. This recall affects specific units with catalog number 01L5:640 and GTIN 380740001193.
Severe thunderstorms caused transit delays for certain cold chain products, leading to improper storage conditions. This could increase the chance of incorrect test results or delayed testing outcomes if the solution was not kept at the correct temperature.
Healthcare facilities using Abbott Diagnostics probe conditioning solution with catalog number 01L5640 or GTIN 380740001193 are likely affected. Patients and staff using these products may face incorrect or delayed test results if the solution was stored outside recommended conditions.
Check for catalog number 01L5640 or GTIN 380740001193 on the product label. The product was sold through specific order numbers and may have been affected by recent thunderstorms.
Verify the catalog number 01L5640 or GTIN 380740001193 on the product label.
The recall is due to transit delays from severe thunderstorms causing cold chain products to be stored outside recommended conditions, which may lead to incorrect or delayed test results.
Check the product label for catalog number 01L5640 or GTIN 380740001193. If affected, monitor test results and contact Abbott Diagnostics for guidance.
The recall does not specify a fix; affected users should check product details and monitor test results.
We’ve drafted a message you can send Abbott Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1841-2025 — Abbott Diagnostics Abbott Diagnostics Hello, I own a Abbott Diagnostics that is covered by recall Z-1841-2025 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.
