Abbott's Multi-Analyte Lvl1&2250UL Cholesterol Control devices may give incorrect results if stored outside recommended conditions due to recent severe thunderstorms. Affected units were sold with specific catalog and GTIN numbers.
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's Multi-Analyte Lvl1&2250UL Cholesterol Control devices may give incorrect or delayed test results if stored outside recommended conditions. This recall is due to transit delays from severe thunderstorms causing some units to be stored improperly.
Severe thunderstorms caused transit delays for some units, leading to improper storage conditions. This could result in incorrect or delayed test results if the devices are not stored within the recommended temperature range.
Users of Abbott's Multi-Analyte Lvl1&2250UL Cholesterol Control devices that were sold with catalog number 88773 or GTIN 893038002036 are affected. Those who have stored these devices outside recommended conditions are at higher risk.
Check for catalog number 88773 or GTIN 893038002036 on the device packaging. The product was sold through specific order numbers including 46108009.
Ensure the device is stored within the recommended temperature range to prevent incorrect or delayed test results.
Severe thunderstorms caused transit delays for some units, leading to improper storage conditions that could result in incorrect or delayed test results.
Check for catalog number 88773 or GTIN 893038002036 on the device packaging. The product was sold with order number 46108009.
No, but ensure the device is stored within the recommended temperature range to prevent incorrect or delayed test results.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1824-2025 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1824-2025 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.
