Labstyle Innovations recalls Dario Blood Glucose Monitoring System Model 1015-05 with Android apps 4.3.0-4.3.2 that may duplicate glucose readings. Affected users should check their app version.
The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may experience duplicate logging of a blood glucose level reading.
Labstyle Innovations is recalling Dario Blood Glucose Monitoring System Model 1015-05 with specific Android app versions because they can duplicate glucose readings. This could lead to inaccurate blood sugar tracking, which might affect diabetes management decisions.
The Android app versions 4.3.0-4.3.2 may log the same blood glucose reading multiple times. This duplication can cause inaccurate readings, potentially leading to incorrect diabetes management decisions.
People using the Dario Blood Glucose Monitoring System Model 1015-05 with Android app versions 4.3.0-4.3.2 are affected. Those with diabetes who rely on accurate glucose readings are most at risk.
Check if your Dario Blood Glucose Monitoring System is Model 1015-05 and has Android app versions 4.3.0-4.3.2. The product was sold with these specific software versions.
Verify your Android app version is 4.3.0-4.3.2 by checking the app settings or description.
The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may experience duplicate logging of a blood glucose level reading.
Check if your Dario Blood Glucose Monitoring System is Model 1015-05 and has Android app versions 4.3.0-4.3.2.
The recall record does not specify a remedy, so you should check your app version and consider updating to a newer version if available.
We’ve drafted a message you can send Labstyle Innovations to request your refund or repair — edit it as you like.
Subject: Recall Z-0260-2020 — Labstyle Innovations Labstyle Innovations Hello, I own a Labstyle Innovations that is covered by recall Z-0260-2020 from Labstyle Innovations. 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.
