Medical Device Recall: LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5
Boston Scientific Corporation · March 30, 2026
Reason for Recall
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.
Distribution
Worldwide distribution - US Nationwide and the country of Belgium.
States Affected
NATIONWIDE
Quantity Affected
2 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2048-2026
Status: ongoing
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