Abbott HbA1c test kits recalled due to transit delays causing improper storage. This may lead to incorrect or delayed test results. Check product details for affected kits.
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 HbA:1c test kits were recalled because severe thunderstorms caused some to be stored outside recommended conditions. This could lead to incorrect or delayed test results, which is important for accurate diabetes management.
Severe thunderstorms caused transit delays, leading some test kits to be stored outside the recommended cold chain conditions. This could increase the chance of incorrect or delayed test results, which is critical for diabetes management.
People using Abbott HbA1c test kits for diabetes monitoring may be affected. Those who have the kits from the specified catalog numbers and GTIN are most at risk.
Check for catalog number 1116974 or GTIN 7070060014654 on the test kit packaging. The kits were sold with order numbers 46085136 and 46115470.
Look for catalog number 1116974 or GTIN 7070060014654 on the test kit packaging.
Severe thunderstorms caused transit delays, leading some kits to be stored outside recommended cold chain conditions, which could increase the chance of incorrect or delayed test results.
Check for catalog number 1116974 or GTIN 7070060014654 on the test kit packaging. The kits were sold with order numbers 46085136 and 46115470.
The recall does not require immediate action, but you should check the product details to confirm if it is affected.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1830-2025 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1830-2025 from Abbott. 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.
