FDAMarch 30, 2026device

LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe), Model 6446, Version 7.5, or SERVER SW LATITUDE DRAGON AU (Australia/New Zealand), Model 6448, Version 7.5

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

The hazard

For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhythmia and Pause (M312 only). In addition, for these devices that are not being monitored, the LATITUDE Clarity programming screens have discrepant information, indicating that the monitoring is enabled for these features in one location and not enabled in another location.

What to do

FDA enforcement status: Ongoing

Brands named

boston scientificboston

UPCs

00802526620706008025266237070080252661382100802526613814

Recall history

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

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