HemoCue recalls Glucose 201 Microcuvettes due to potential incorrect or delayed test results from improper storage. Affected units may not be safe for accurate blood glucose testing.
Glucose microcuvettes experienced transit time outside of limits, so stability through the whole microcuvette lifetime can no longer be guaranteed. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency, and purity of the product. This failure could increase the probability of an incorrect test result or a delayed test result.
HemoCue is recalling Glucose 201 Microcuvettes because they may not work properly if stored incorrectly, leading to inaccurate or delayed blood glucose test results. This could affect people using these test strips for diabetes management.
The microcuvettes may not stay stable if stored outside recommended conditions, which can cause incorrect or delayed test results. This means blood glucose readings might be too high or too low, affecting diabetes management.
People using HemoCue Glucose 201 Microcuvettes for blood glucose testing are affected. Those with diabetes who rely on these test strips for monitoring are most at risk.
Check for the HemoCue Glucose 201 Microcuvettes with UDI-DI: 07311091107060 and Lot: 2501708. Only 4 boxes were shipped through McKesson.
Ensure the microcuvettes are stored at the recommended temperature and humidity levels as labeled.
Look for the UDI-DI code 07311091107060 and lot number 2501708 on the packaging.
The microcuvettes may not stay stable if stored outside recommended conditions, which could cause incorrect or delayed blood glucose test results.
This recall is for potential inaccurate test results, not physical harm. The risk is low and only affects test accuracy.
Check for the UDI-DI code 07311091107060 and lot number 2501708 on the packaging. Only 4 boxes were shipped through McKesson.
We’ve drafted a message you can send HemoCue to request your refund or repair — edit it as you like.
Subject: Recall Z-2070-2025 — HemoCue HemoCue Hello, I own a HemoCue that is covered by recall Z-2070-2025 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.
