Ortho Clinical Diagnostics recalls Diluent Pack 3 due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Consumers should check product details and contact the manufacturer.
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.
Ortho Clinical Diagnostics is recalling Diluent Pack 3 products because severe thunderstorms caused some to be stored outside recommended conditions. This could lead to incorrect or delayed test results if used.
Severe thunderstorms caused transit delays for some products, leading them to be stored outside the recommended cold chain conditions. This could increase the chance of incorrect or delayed test results when used.
People who own or use Ortho Clinical Diagnostics Diluent Pack 3 products for medical testing may be affected. Those with recent test results could be at higher risk if the product was stored improperly.
Check for the product name 'Diluent Pack 3' with catalog number 6801754 or GTIN 1075:8750007004. Products were sold through Mckesson Medical-Surgical Inc. Corporate Office.
Look for catalog number 6801754 or GTIN 10758750007004 on the product label.
Severe thunderstorms caused transit delays for some products, leading them to be stored outside recommended cold chain conditions. This could increase the chance of incorrect or delayed test results.
Check for the product name 'Diluent Pack 3' with catalog number 6801754 or GTIN 10758750007004. Products were sold through Mckesson Medical-Surgical Inc. Corporate Office.
The recall record does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Ortho Clinical Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1834-2025 — Ortho Clinical Diagnostics Ortho Clinical Diagnostics Hello, I own a Ortho Clinical Diagnostics that is covered by recall Z-1834-2025 from Ortho Clinical 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.
