Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D SDM-00001-3D SDM-05000-3D3 SDM-05000-2DC SDM-00001-M3D SDM-05000-3DC SDM-SYS-6000-3D SDM-05000-2D3 SDA-SYS-3000-2D SDM-00001 SDM-SYS-9000-2D SDM-00001-M2D 3DM-SYS-STD 3DM-SYS-STD-NS SDM-05000-2AC SDM-05000-2A2 SDA-SYS-3000-3D SDA-SYS-3000-3D-UPS SDM-SYS-6000-3D-HTC SDM-05000-2D2 SDM-05000-3D2 SDM-SYS-6000-2D SDM-SYS-9000-3D
FDA Recall Z-1144-2023 · Posted 2023-02-21
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Recalling FirmHologic, Inc.
Recall StatusOpen, Classified
Product CodeOTE
Date Initiated2023-01-16
Product Quantity797 units
Reason for Recall
C-Arm unexpected movement may cause blunt trauma should the tube arm impinge upon an individual
Firm Action
Hologic issued Urgent Medical Device Correction Letter customized to the customer on 01/16/23. Letter states reason for recall, health risk and action to take:
We will schedule a service appointment and dispatch a field service engineer to visit your site to inspect your system and if necessary, make any corrections.
" This will take approximately 6-14 hours to complete.
" Until your service appointment, you will be able to continue to use your Selenia Dimensions or 3Dimensions system.
If at any time during system operation, you observe any unanticipated error messages, or unexpected Carm movement, please discontinue use and contact Hologic's Technical Support immediately.
Additionally, if you have any questions, please do not hesitate to reach out to Hologic's Technical Support at 1-877-371-4372 or [email protected].
Complete the on line Customer Confirmation Form using the link below within 3 business days of receiving this notice. Replying promptly will confirm your receipt of the notification and prevent you from receiving repeat notices.
www.novasyte.com/hologic/selenia-dimensions-2022
Root Cause
Device Design
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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