Selenia Dimensions 2d/3d Mammography Systems

Selenia Dimensions 2D/3D Mammography Systems Recall Hologic is recalling Selenia Dimensions 2D/3D Mammography Systems in Canada due to a device performance issue. This recall affects mammography systems distributed across Canada. The FDA classified this as a Class II recall.

Product
Selenia Dimensions 2D/3D Mammography Systems
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-06-10
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b9e449f2-5c17-4add-8a4d-6ef96469237a