Boston Scientific recalls myLUX Patient Application version 2.0.101 and 2.0.110 for Apple devices due to potential data transmission failure from cardiac monitors.
Patients using the Model 2939 myLUX Patient Application on their Apple mobile device (e.g., iPhone) may not be transmitting data from their Insertable Cardiac Monitor to the LATITUDE Clarity website.
Boston Scientific is recalling their myLUX Patient Application for Apple devices (model 2939, versions 2.0.101 and 2.0.110) because it may not transmit data from the patient's cardiac monitor to the LATITUDE Clarity website. This could affect patients using the app to monitor their heart health.
The app may fail to send data from the patient's cardiac monitor to the LATITUDE Clarity website. This could prevent patients from monitoring their heart health through the app. However, the hazard does not involve immediate physical danger.
Patients using the myLUX Patient Application on Apple devices (iPhone) with model 2939, versions 2.0.101 or 2.0.110 are affected. Those with insertable cardiac monitors are most at risk.
Check your Apple device for the myLUX Patient Application version 2.0.101 or 2.0.110. The product is sold with model number 2939 and GTIN 00802526618215.
Update to the latest version of the myLUX Patient Application to ensure data transmission works properly.
The app may not transmit data from the patient's cardiac monitor to the LATITUDE Clarity website, which could affect heart health monitoring.
The recall does not mention any risk of serious injury; the hazard is limited to potential data transmission failure.
Check your Apple device for the myLUX Patient Application version 2.0.101 or 2.0.110 with model number 2939.
We’ve drafted a message you can send Boston Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-0226-2025 — Boston Scientific Boston Scientific Hello, I own a Boston Scientific that is covered by recall Z-0226-2025 from Boston Scientific. 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.
