FDASeptember 6, 2024device

Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version 2.0.101, 2.0.110, cardiac monitor application.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

00802526618215

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version 2.0.101, 2.0.110, cardiac monitor application. — Recall Details · AllClear