Ortho Clinical Diagnostics recalls Vitros BUN reagents due to transit delays during thunderstorms causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected items.
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 Vitros BUN reagents because severe thunderstorms caused transit delays, potentially leading to improper storage conditions. This could result in incorrect or delayed test results if the reagents are used after being exposed to temperatures outside the recommended range.
The reagents were stored outside recommended temperature conditions due to transit delays caused by severe thunderstorms. This improper storage could lead to incorrect or delayed test results when used in clinical testing.
Users of Vitros BUN reagents who purchased them from Mckesson Medical-Surgical Inc. or other authorized sellers. Healthcare professionals and labs using these reagents are most at risk of inaccurate test results.
Check for the product name 'Vitros BUN (60/CR 5CR/PK) ORCLNL REAGENT' with catalog number 8102204 and GTIN 10758750004362. These reagents were sold through Mckesson Medical-Surgical Inc. or other authorized channels.
Verify the product name, catalog number, and GTIN to confirm if your reagent is affected.
Severe thunderstorms caused transit delays, leading to improper storage conditions that could increase the risk of incorrect or delayed test results.
Check for the product name 'Vitros BUN (60/CR 5CR/PK) ORCLNL REAGENT' with catalog number 8102204 and GTIN 10758750004362.
The recall does not specify a remedy, so you should check with your supplier or healthcare provider for 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-1837-2025 — Ortho Clinical Diagnostics Ortho Clinical Diagnostics Hello, I own a Ortho Clinical Diagnostics that is covered by recall Z-1837-2025 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.
