Ortho Clinical Diagnostics recalls Vancomycin reagent due to transit delays from thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details to see if affected.
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 Vancomycin reagent products because thunderstorms caused transit delays, leading to improper storage conditions. This could result in incorrect or delayed test results if the reagent is used.
Thunderstorms caused transit delays for certain cold chain products, meaning the reagents were stored outside recommended temperature conditions. This improper storage could lead to incorrect or delayed test results when used.
Healthcare facilities that use Ortho Clinical Diagnostics Vancomycin reagent products are likely affected. Patients receiving tests using these reagents may be at risk of incorrect or delayed results.
Check for the product name 'Vancomycin (300/BX)ORCLNL Reagent' with catalog number 6801709 or GTIN 10758750006731. Products were sold through Mckesson Medical-Surgical Inc. Corporate Office.
Identify if your reagent has catalog number 6801709 or GTIN 10758750006731.
Thunderstorms caused transit delays, leading to improper storage conditions that could increase the chance of incorrect or delayed test results.
Check if your reagent has catalog number 6801709 or GTIN 10758750006731. If affected, contact your supplier for guidance.
The recall does not provide a specific remedy; affected products should be checked and handled according to the manufacturer's guidance.
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-1833-2025 — Ortho Clinical Diagnostics Ortho Clinical Diagnostics Hello, I own a Ortho Clinical Diagnostics that is covered by recall Z-1833-2025 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.
