Recall of Abbott Architect Vitamin D 6-Level Calibrator due to transit delays causing improper storage. 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 Diagnostics is recalling its Vitamin D 6-Level Calibrator devices because severe thunderstorms caused transit delays, potentially leading to improper storage. This could result in incorrect or delayed test results if the device is used after the recall.
Severe thunderstorms caused transit delays for certain cold chain products. This led to the devices being stored outside recommended temperature conditions. As a result, the devices might produce incorrect or delayed test results.
Healthcare facilities using the Abbott Architect Vitamin D 6-Level Calibrator may be affected. Laboratories and clinics that handle this specific device are most at risk.
Check for the product name 'Abbott Architect Vitamin D 6-Level Calibrator', catalog number 05P0202, or GTIN 38074:142742. The device was sold with order number 46048552.
Verify the product name, catalog number, GTIN, or order number to confirm if your device is affected.
Severe thunderstorms caused transit delays, leading to improper storage conditions that could increase the risk of incorrect or delayed test results.
Check the product details to confirm if your device is affected. If it is, you may need to contact Abbott Diagnostics for further instructions.
The recall record does not mention a specific remedy or fix for this issue.
We’ve drafted a message you can send Abbott Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1848-2025 — Abbott Diagnostics Abbott Diagnostics Hello, I own a Abbott Diagnostics that is covered by recall Z-1848-2025 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.
