Abbott Diabetes Care recalls FreeStyle Libre 3 Plus sensors with specific serial numbers due to potential carbon buildup causing incorrect low glucose readings. Affected units may need replacement to ensure accurate blood sugar monitoring.
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
Abbott Diabetes Care is recalling FreeStyle Libre 3 Plus sensors that may cause incorrect low glucose results due to carbon buildup from a manufacturing issue. This could lead to inaccurate blood sugar readings if the sensor is used without replacement.
A manufacturing process issue can cause carbon buildup in the sensor, which may lead to incorrect low glucose results. This could cause users to misinterpret their blood sugar levels, potentially leading to unsafe decisions about their diabetes management.
People who own or use the FreeStyle Libre 3 Continuous Glucose Monitoring System with the recalled sensor model (REF 78769-01 UDI-DI code: 00357599843014) are affected. Those with diabetes who rely on this sensor for blood glucose monitoring are most at risk.
Check if your FreeStyle Libre 3 Plus sensor has the model number REF 78769-01 and UDI-DI code 00357599843014. The product was sold from 2023 to 2026 with specific serial numbers listed in the recall notice.
Verify your sensor's model number (REF 78769-01) and UDI-DI code (00357599843014) to see if it's affected.
If your sensor is affected, replace it with a new one to ensure accurate glucose readings.
Due to a manufacturing process issue that may cause carbon buildup in the sensor, leading to incorrect low glucose results.
Check your sensor's model number (REF 78769-01) and UDI-DI code (00357599843014). Affected units have specific serial numbers listed in the recall notice.
No, but if your sensor is affected, you should replace it to ensure accurate glucose readings.
We’ve drafted a message you can send Abbott Diabetes Care to request your refund or repair — edit it as you like.
Subject: Recall Z-1022-2026 — Abbott Diabetes Care Abbott Diabetes Care Hello, I own a Abbott Diabetes Care that is covered by recall Z-1022-2026 from Abbott Diabetes Care. 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.
