HEMOCUE Glucose Test Kits may give incorrect results if stored outside recommended conditions due to transit delays from thunderstorms. Affected kits include specific model numbers and order details.
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.
HEMOCUE Glucose Test Kits with catalog number 180.013.002 may give incorrect or delayed test results if stored outside recommended conditions. This recall is due to transit delays from severe thunderstorms causing some kits to be stored improperly.
Severe thunderstorms caused transit delays for some kits, leading to improper storage conditions. This can increase the chance of incorrect or delayed glucose test results, which may affect patient monitoring.
Healthcare providers using HEMOCUE Glucose Test Kits with catalog number 180.013.002 are most at risk. Patients relying on these kits for glucose monitoring could see inaccurate results if the kits were stored improperly.
Check for catalog number 180.013.002 on the HEMOCUE Glucose Test Kit. The kit was sold with GTIN 8718734960935 and order number 46096008.
Ensure the kit is stored within the recommended temperature and humidity conditions if you have it.
The recall is due to transit delays from severe thunderstorms causing some kits to be stored outside recommended conditions, which may lead to incorrect or delayed test results.
The affected model is catalog number 180.013.002 with GTIN 8718734960935 and order number 46096008.
No, but you should check if the kit has been stored properly. If it was stored outside recommended conditions, it may give incorrect results.
We’ve drafted a message you can send HEMOCUE to request your refund or repair — edit it as you like.
Subject: Recall Z-1855-2025 — HEMOCUE HEMOCUE Hello, I own a HEMOCUE that is covered by recall Z-1855-2025 from HEMOCUE. 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.
